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Single-Use Endoscopic Scissors

FDA UDI

Class I (US FDA UDI)

by Guangzhou Red Pine Medical Instrument Co., Ltd.

Identity

Trade Name
Single-Use Endoscopic Scissors FDA UDI
Generic Name
Rigid endoscopic scissors, single-use FDA UDI
Model / Reference
RP-G-H01 FDA UDI

Identifiers

Primary DI / UDI-DI
06972520301650 FDA UDI
FDA Product Code
NWW FDA UDI
GMDN Term
Rigid endoscopic scissors, single-use 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Category: Rigid endoscopic scissors, single-use

Single-Use Endoscopic Scissors by Guangzhou Red Pine Medical Instrument Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid endoscopic scissors, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c2f3c103-8dcb-452c-8a1e-db76ea94158b 32 fields · synced Jun 1, 2026