EUDAMED last updated this device on Mar 27, 2026

Upgrade to MR 7700

0884838BM697TZ

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Philips Medical Systems Nederland B.V.
UDI-DI code: 00884838115781
Reference / catalog number: 782167

Upgrade to MR 7700 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by Philips Medical Systems Nederland B.V.. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

Role
Country
Date of registration
Address

EUDAMED last updated this device on Mar 27, 2026

Upgrade to MR 7700

0884838BM697TZ

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Philips Medical Systems Nederland B.V.
UDI-DI code: 00884838115781
Reference / catalog number: 782167

View device family (Basic UDI)

Device identification

Trade name: Upgrade to MR 7700
UDI-DI code: 00884838115781
Basic UDI-DI: 0884838BM697TZ
Reference / catalog number: 782167
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Upgrade to the MR 7700 gradient performance for customers having an Elition X
Additional information URL: https://www.philips.nl/healthcare/over-ons/support/resource-center/results#sort=relevancy&f:@ps_contenttype=[Instruction%20for%20Use]&f:@ps_modality=[Magnetic%20resonance%20(MRI)]&f:@ps_language=[English%20(US)]
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)00884838115781

UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Z11050105CLOSED MAGNET MRI SCANNERS WITH MAGNETIC FIELD GREATER THAN 2T AND LESS THAN OR EQUAL TO 4T

Critical warnings

No critical warnings reported for this device.

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

Certificates covering this device

No certificate specifically references this device's Basic UDI-DI.

Market distribution

Primary placement in Netherlands; available across 32 countries total.

Country	On market since	Until
NetherlandsPrimary placement	Jan 9, 2025	Dec 31, 9999
Türkiye		Still on market
XI		Still on market
Austria	Jan 9, 2025	Dec 31, 9999
Belgium	Jan 9, 2025	Dec 31, 9999
Bulgaria	Jan 9, 2025	Dec 31, 9999
Cyprus	Jan 9, 2025	Dec 31, 9999
Czechia	Jan 9, 2025	Dec 31, 9999
Germany	Jan 9, 2025	Dec 31, 9999
Denmark	Jan 9, 2025	Dec 31, 9999
Estonia	Jan 9, 2025	Dec 31, 9999
EL	Jan 9, 2025	Dec 31, 9999
Spain	Jan 9, 2025	Dec 31, 9999
Finland	Jan 9, 2025	Dec 31, 9999
France	Jan 9, 2025	Dec 31, 9999
Croatia	Jan 9, 2025	Dec 31, 9999
Hungary	Jan 9, 2025	Dec 31, 9999
Ireland	Jan 9, 2025	Dec 31, 9999
Iceland	Jan 9, 2025	Dec 31, 9999
Italy	Jan 9, 2025	Dec 31, 9999
Liechtenstein	Jan 9, 2025	Dec 31, 9999
Lithuania	Jan 9, 2025	Dec 31, 9999
Luxembourg	Jan 9, 2025	Dec 31, 9999
Latvia	Jan 9, 2025	Dec 31, 9999
Malta	Jan 9, 2025	Dec 31, 9999
Norway	Jan 9, 2025	Dec 31, 9999
Poland	Jan 9, 2025	Dec 31, 9999
Portugal	Jan 9, 2025	Dec 31, 9999
Romania	Jan 9, 2025	Dec 31, 9999
Sweden	Jan 9, 2025	Dec 31, 9999
Slovenia	Jan 9, 2025	Dec 31, 9999
Slovakia	Jan 9, 2025	Dec 31, 9999

Device identification

Trade name: Upgrade to MR 7700
UDI-DI code: 00884838115781
Basic UDI-DI: 0884838BM697TZ
Reference / catalog number: 782167
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Upgrade to the MR 7700 gradient performance for customers having an Elition X
Additional information URL: https://www.philips.nl/healthcare/over-ons/support/resource-center/results#sort=relevancy&f:@ps_contenttype=[Instruction%20for%20Use]&f:@ps_modality=[Magnetic%20resonance%20(MRI)]&f:@ps_language=[English%20(US)]
Clinical sizes: No clinical sizes registered for this device.

Manufacturer information

Organization name: Philips Medical Systems Nederland B.V.
SRN: NL-MF-000001489
Manufacturer status: Active

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)00884838115781

UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Z11050105CLOSED MAGNET MRI SCANNERS WITH MAGNETIC FIELD GREATER THAN 2T AND LESS THAN OR EQUAL TO 4T

Critical warnings

No critical warnings reported for this device.

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

Certificates

Certificate health across this manufacturer's portfolio.

HZ 1135905-1Issued
Quality management systemNotified body: 0197Expiry: Jun 4, 2030

Certificates covering this device

No certificate specifically references this device's Basic UDI-DI.

All products by Philips Medical Systems Nederland B.V.

Market distribution

Primary placement in Netherlands; available across 32 countries total.

Country	On market since	Until
NetherlandsPrimary placement	Jan 9, 2025	Dec 31, 9999
Türkiye		Still on market
XI		Still on market
Austria	Jan 9, 2025	Dec 31, 9999
Belgium	Jan 9, 2025	Dec 31, 9999
Bulgaria	Jan 9, 2025	Dec 31, 9999
Cyprus	Jan 9, 2025	Dec 31, 9999
Czechia	Jan 9, 2025	Dec 31, 9999
Germany	Jan 9, 2025	Dec 31, 9999
Denmark	Jan 9, 2025	Dec 31, 9999
Estonia	Jan 9, 2025	Dec 31, 9999
EL	Jan 9, 2025	Dec 31, 9999
Spain	Jan 9, 2025	Dec 31, 9999
Finland	Jan 9, 2025	Dec 31, 9999
France	Jan 9, 2025	Dec 31, 9999
Croatia	Jan 9, 2025	Dec 31, 9999
Hungary	Jan 9, 2025	Dec 31, 9999
Ireland	Jan 9, 2025	Dec 31, 9999
Iceland	Jan 9, 2025	Dec 31, 9999
Italy	Jan 9, 2025	Dec 31, 9999
Liechtenstein	Jan 9, 2025	Dec 31, 9999
Lithuania	Jan 9, 2025	Dec 31, 9999
Luxembourg	Jan 9, 2025	Dec 31, 9999
Latvia	Jan 9, 2025	Dec 31, 9999
Malta	Jan 9, 2025	Dec 31, 9999
Norway	Jan 9, 2025	Dec 31, 9999
Poland	Jan 9, 2025	Dec 31, 9999
Portugal	Jan 9, 2025	Dec 31, 9999
Romania	Jan 9, 2025	Dec 31, 9999
Sweden	Jan 9, 2025	Dec 31, 9999
Slovenia	Jan 9, 2025	Dec 31, 9999
Slovakia	Jan 9, 2025	Dec 31, 9999

Upgrade to MR 7700

Upgrade to MR 7700

Device identification

Classification

Device details

UDI-PI traceability

UDI-DI DataMatrix

UDI-PI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Substances

Regulatory

Lifecycle

Certificates covering this device

Market distribution

Related searches

Device identification

Classification

Device details

Manufacturer information

UDI-PI traceability

UDI-DI DataMatrix

UDI-PI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Substances

Regulatory

Lifecycle

Certificates

Certificates covering this device

Related devices

Market distribution

Related searches

Manufacturer information

Certificates

Related devices