Organization name

Zhuji Pengtian Medical Instrument Co.,Ltd

SRN

CN-MF-000013084

Manufacturer status

Active

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

• Caution

  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.

Primary placement in Austria; available across 32 countries total.

Trade name

not provided

UDI-DI code

Primary DI

The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.

06950190410520

Basic UDI-DI

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

69501904biopsyforceps01QY

Reference / catalog number

PTY1-2320T

Issuing entity

UDI issuing entities

Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.

GS1

Risk category

MDR risk classes

MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.

Class IIa

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

1

Additional product description

Sterile

Additional information URL

https://www.pengtianmed.com/

Clinical sizes

No clinical sizes registered for this device.

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

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

• G03080199GASTROINTESTINAL ENDOSCOPY, FORCEPS, SINGLE-USE - OTHER

• Class IIa medical devices in EUDAMED

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