EUDAMED last updated this device on Nov 18, 2025

IQ

4039239000001062ZR

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Aesculap AG
UDI-DI code: 04046964253553
Reference / catalog number: NS407R

View device family (Basic UDI)

Role
Country
Date of registration
Address

EUDAMED last updated this device on Nov 18, 2025

IQ

4039239000001062ZR

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Aesculap AG
UDI-DI code: 04046964253553
Reference / catalog number: NS407R

View device family (Basic UDI)

Device identification

Trade name: IQ
UDI-DI code: 04046964253553
Basic UDI-DI: 4039239000001062ZR
Reference / catalog number: NS407R
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: IQ MEDIALIZED TIBIA CUTTING GUIDE RIGHT
Additional information URL: https://eifu.bbraun.com/
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)04046964253553

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.

L091199ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER

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 Germany; available across 27 countries total.

Country	On market since	Until
GermanyPrimary placement	Aug 5, 2013	Still on market
Austria	Aug 5, 2013	Still on market
Belgium	Aug 5, 2013	Still on market
Bulgaria	Aug 5, 2013	Still on market
Cyprus	Aug 5, 2013	Still on market
Czechia	Aug 5, 2013	Still on market
Denmark	Aug 5, 2013	Still on market
Estonia	Aug 5, 2013	Still on market
EL	Aug 5, 2013	Still on market
Spain	Aug 5, 2013	Still on market
Finland	Aug 5, 2013	Still on market
France	Aug 5, 2013	Still on market
Croatia	Aug 5, 2013	Still on market
Hungary	Aug 5, 2013	Still on market
Ireland	Aug 5, 2013	Still on market
Italy	Aug 5, 2013	Still on market
Lithuania	Aug 5, 2013	Still on market
Luxembourg	Aug 5, 2013	Still on market
Latvia	Aug 5, 2013	Still on market
Malta	Aug 5, 2013	Still on market
Netherlands	Aug 5, 2013	Still on market
Poland	Aug 5, 2013	Still on market
Portugal	Aug 5, 2013	Still on market
Romania	Aug 5, 2013	Still on market
Sweden	Aug 5, 2013	Still on market
Slovenia	Aug 5, 2013	Still on market
Slovakia	Aug 5, 2013	Still on market

Device identification

Trade name: IQ
UDI-DI code: 04046964253553
Basic UDI-DI: 4039239000001062ZR
Reference / catalog number: NS407R
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: IQ MEDIALIZED TIBIA CUTTING GUIDE RIGHT
Additional information URL: https://eifu.bbraun.com/
Clinical sizes: No clinical sizes registered for this device.

Manufacturer information

Organization name: Aesculap AG
SRN: DE-MF-000005504
Manufacturer status: Active

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)04046964253553

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.

L091199ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER

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.

G12 010066 0441Supplemented
Quality management systemNotified body: 0123Expiry: Jun 30, 2026
20334GB450240524Issued
Technical documentationNotified body: 0482Expiry: May 23, 2029
20333GB450240524Issued
Technical documentationNotified body: 0482Expiry: May 23, 2029

Certificates covering this device

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

Market distribution

Primary placement in Germany; available across 27 countries total.

Country	On market since	Until
GermanyPrimary placement	Aug 5, 2013	Still on market
Austria	Aug 5, 2013	Still on market
Belgium	Aug 5, 2013	Still on market
Bulgaria	Aug 5, 2013	Still on market
Cyprus	Aug 5, 2013	Still on market
Czechia	Aug 5, 2013	Still on market
Denmark	Aug 5, 2013	Still on market
Estonia	Aug 5, 2013	Still on market
EL	Aug 5, 2013	Still on market
Spain	Aug 5, 2013	Still on market
Finland	Aug 5, 2013	Still on market
France	Aug 5, 2013	Still on market
Croatia	Aug 5, 2013	Still on market
Hungary	Aug 5, 2013	Still on market
Ireland	Aug 5, 2013	Still on market
Italy	Aug 5, 2013	Still on market
Lithuania	Aug 5, 2013	Still on market
Luxembourg	Aug 5, 2013	Still on market
Latvia	Aug 5, 2013	Still on market
Malta	Aug 5, 2013	Still on market
Netherlands	Aug 5, 2013	Still on market
Poland	Aug 5, 2013	Still on market
Portugal	Aug 5, 2013	Still on market
Romania	Aug 5, 2013	Still on market
Sweden	Aug 5, 2013	Still on market
Slovenia	Aug 5, 2013	Still on market
Slovakia	Aug 5, 2013	Still on market

IQ

IQ

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