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Single use grasping forceps PGA

FDA UDI

Class II (US FDA UDI)

by Zhuhai Pusen Medical Technology Co, Ltd

Identity

Trade Name
Single use grasping forceps PGA FDA UDI
Generic Name
Flexible endoscopic tissue manipulation forceps, single-use FDA UDI
Device Name
The single use grasping forceps is intended to be used through working channel of endoscope to remove foreign bodies. FDA UDI
Model / Reference
PGA FDA UDI
Description
The single use grasping forceps is intended to be used through working channel of endoscope to remove foreign bodies. FDA UDI

Identifiers

Primary DI / UDI-DI
06971176281545 FDA UDI
FDA Product Code
PTS FDA UDI
GMDN Term
Flexible endoscopic tissue manipulation forceps, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Flexible endoscopic tissue manipulation forceps, single-use

Single use grasping forceps PGA by Zhuhai Pusen Medical Technology Co, Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible endoscopic tissue manipulation forceps, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zhuhai Pusen Medical Technology Co, Ltd

Sources (1)

  • FDA UDI 4ac7638b-88ff-4ffb-b543-0c56a3ef03bb 33 fields · synced Jun 1, 2026