← Back to catalogue

OriGynMED

FDA UDI

Class I (US FDA UDI)

by OriGyn Medical Technology (Hangzhou) Co., Ltd.

Identity

Trade Name
OriGynMED FDA UDI
Generic Name
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI
Model / Reference
YZ211.044 FDA UDI

Identifiers

Primary DI / UDI-DI
06976860690443 FDA UDI
FDA Product Code
NWW FDA UDI
GMDN Term
Rigid endoscopic tissue manipulation forceps, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.1690 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Rigid endoscopic tissue manipulation forceps, reusable

OriGynMED by OriGyn Medical Technology (Hangzhou) Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid endoscopic tissue manipulation forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
OriGyn Medical Technology (Hangzhou) Co., Ltd.

Sources (1)

  • FDA UDI 5e1ced94-2ba5-420c-a269-35402a1c5359 32 fields · synced May 31, 2026