EUDAMED last updated this device on May 15, 2026

PTY1-2323T

69501904biopsyforceps01QY

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Zhuji Pengtian Medical Instrument Co.,Ltd
UDI-DI code: 06950190412258
Reference / catalog number: PTY1-2323T

View device family (Basic UDI)

Role
Country
Date of registration
Address

EUDAMED last updated this device on May 15, 2026

PTY1-2323T

69501904biopsyforceps01QY

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Zhuji Pengtian Medical Instrument Co.,Ltd
UDI-DI code: 06950190412258
Reference / catalog number: PTY1-2323T

View device family (Basic UDI)

Device identification

Trade name: not provided
UDI-DI code: 06950190412258
Basic UDI-DI: 69501904biopsyforceps01QY
Reference / catalog number: PTY1-2323T
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: Sterile
Additional information URL: https://www.pengtianmed.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)06950190412258

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.

G03080199GASTROINTESTINAL ENDOSCOPY, FORCEPS, SINGLE-USE - OTHER

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW011
1.It must be performed by a trained physician. 2.The minimum through clamp for disposable biopsy forceps is 2.0mm. 3.Do not use if the package is damaged and expired. 4.The product is for single use only, it is strictly prohibited to reuse and has to be disposed after use.

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 Austria; available across 32 countries total.

Country	On market since	Until
AustriaPrimary placement	Feb 17, 2020	Dec 31, 2029
Belgium	Feb 17, 2020	Dec 31, 2029
Bulgaria	Feb 17, 2020	Dec 31, 2029
Cyprus	Feb 17, 2020	Dec 31, 2029
Czechia	Feb 17, 2020	Dec 31, 2029
Germany	Feb 17, 2020	Dec 31, 2029
Denmark	Feb 17, 2020	Dec 31, 2029
Estonia	Feb 17, 2020	Dec 31, 2029
EL	Feb 17, 2020	Dec 31, 2029
Spain	Feb 17, 2020	Dec 31, 2029
Finland	Feb 17, 2020	Dec 31, 2029
France	Feb 17, 2020	Dec 31, 2029
Croatia	Feb 17, 2020	Dec 31, 2029
Hungary	Feb 17, 2020	Dec 31, 2029
Ireland	Feb 17, 2020	Dec 31, 2029
Iceland	Feb 17, 2020	Dec 31, 2029
Italy	Feb 17, 2020	Dec 31, 2029
Liechtenstein	Feb 17, 2020	Dec 31, 2029
Lithuania	Feb 17, 2020	Dec 31, 2029
Luxembourg	Feb 17, 2020	Dec 31, 2029
Latvia	Feb 17, 2020	Dec 31, 2029
Malta	Feb 17, 2020	Dec 31, 2029
Netherlands	Feb 17, 2020	Dec 31, 2029
Norway	Feb 17, 2020	Dec 31, 2029
Poland	Feb 17, 2020	Dec 31, 2029
Portugal	Feb 17, 2020	Dec 31, 2029
Romania	Feb 17, 2020	Dec 31, 2029
Sweden	Feb 17, 2020	Dec 31, 2029
Slovenia	Feb 17, 2020	Dec 31, 2029
Slovakia	Feb 17, 2020	Dec 31, 2029
Türkiye	Feb 17, 2020	Dec 31, 2029
XI	Feb 17, 2020	Dec 31, 2029

Device identification

Trade name: not provided
UDI-DI code: 06950190412258
Basic UDI-DI: 69501904biopsyforceps01QY
Reference / catalog number: PTY1-2323T
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: Sterile
Additional information URL: https://www.pengtianmed.com/
Clinical sizes: No clinical sizes registered for this device.

Manufacturer information

Organization name: Zhuji Pengtian Medical Instrument Co.,Ltd
SRN: CN-MF-000013084
Manufacturer status: Active

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)06950190412258

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.

G03080199GASTROINTESTINAL ENDOSCOPY, FORCEPS, SINGLE-USE - OTHER

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW011
1.It must be performed by a trained physician. 2.The minimum through clamp for disposable biopsy forceps is 2.0mm. 3.Do not use if the package is damaged and expired. 4.The product is for single use only, it is strictly prohibited to reuse and has to be disposed after use.

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

No certificates registered for this manufacturer.

Certificates covering this device

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

Market distribution

Primary placement in Austria; available across 32 countries total.

Country	On market since	Until
AustriaPrimary placement	Feb 17, 2020	Dec 31, 2029
Belgium	Feb 17, 2020	Dec 31, 2029
Bulgaria	Feb 17, 2020	Dec 31, 2029
Cyprus	Feb 17, 2020	Dec 31, 2029
Czechia	Feb 17, 2020	Dec 31, 2029
Germany	Feb 17, 2020	Dec 31, 2029
Denmark	Feb 17, 2020	Dec 31, 2029
Estonia	Feb 17, 2020	Dec 31, 2029
EL	Feb 17, 2020	Dec 31, 2029
Spain	Feb 17, 2020	Dec 31, 2029
Finland	Feb 17, 2020	Dec 31, 2029
France	Feb 17, 2020	Dec 31, 2029
Croatia	Feb 17, 2020	Dec 31, 2029
Hungary	Feb 17, 2020	Dec 31, 2029
Ireland	Feb 17, 2020	Dec 31, 2029
Iceland	Feb 17, 2020	Dec 31, 2029
Italy	Feb 17, 2020	Dec 31, 2029
Liechtenstein	Feb 17, 2020	Dec 31, 2029
Lithuania	Feb 17, 2020	Dec 31, 2029
Luxembourg	Feb 17, 2020	Dec 31, 2029
Latvia	Feb 17, 2020	Dec 31, 2029
Malta	Feb 17, 2020	Dec 31, 2029
Netherlands	Feb 17, 2020	Dec 31, 2029
Norway	Feb 17, 2020	Dec 31, 2029
Poland	Feb 17, 2020	Dec 31, 2029
Portugal	Feb 17, 2020	Dec 31, 2029
Romania	Feb 17, 2020	Dec 31, 2029
Sweden	Feb 17, 2020	Dec 31, 2029
Slovenia	Feb 17, 2020	Dec 31, 2029
Slovakia	Feb 17, 2020	Dec 31, 2029
Türkiye	Feb 17, 2020	Dec 31, 2029
XI	Feb 17, 2020	Dec 31, 2029

PTY1-2323T

PTY1-2323T

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