EUDAMED last updated this device on Apr 22, 2026

Flexible Videoscopes

697028348UE000029JM

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Zhejiang UE Medical Corp.
UDI-DI code: 06937048212451
Reference / catalog number: EBM-120T2LR

Flexible Videoscopes is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Zhejiang UE Medical Corp.. Placed on the EU market in Spain. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

Role
Country
Date of registration
Address

EUDAMED last updated this device on Apr 22, 2026

Flexible Videoscopes

697028348UE000029JM

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Zhejiang UE Medical Corp.
UDI-DI code: 06937048212451
Reference / catalog number: EBM-120T2LR

View device family (Basic UDI)

Device identification

Trade name: Flexible Videoscopes
UDI-DI code: 06937048212451
Basic UDI-DI: 697028348UE000029JM
Reference / catalog number: EBM-120T2LR
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: The Flexible Videoscopes is used to guide the endotracheal intubation and used for rhinopharyngeal and oropharyngeal examination.
Additional information URL: No additional information URL provided by the manufacturer.
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)06937048212451

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.

Z12021006VIDEO NASOPHARYNGO/LARYNGOSCOPES

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 Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement		Still on market

Device identification

Trade name: Flexible Videoscopes
UDI-DI code: 06937048212451
Basic UDI-DI: 697028348UE000029JM
Reference / catalog number: EBM-120T2LR
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: The Flexible Videoscopes is used to guide the endotracheal intubation and used for rhinopharyngeal and oropharyngeal examination.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

Manufacturer information

Organization name: Zhejiang UE Medical Corp.
SRN: CN-MF-000003020
Manufacturer status: Active

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)06937048212451

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.

Z12021006VIDEO NASOPHARYNGO/LARYNGOSCOPES

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 2028023-1Supplemented
Quality management systemNotified body: 0197Expiry: Nov 6, 2029

Certificates covering this device

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

All products by Zhejiang UE Medical Corp.

Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement		Still on market

Flexible Videoscopes

Flexible Videoscopes

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