← Back to catalogue

Redpine

FDA UDI

Class I (US FDA UDI)

by Guangzhou Red Pine Medical Instrument Co., Ltd.

Identity

Trade Name
REDPINE FDA UDI
Generic Name
Rigid endoscopic biopsy forceps, single-use FDA UDI
Model / Reference
RP-U-P1502 FDA UDI

Identifiers

Primary DI / UDI-DI
06972520300943 FDA UDI
FDA Product Code
FCL FDA UDI
GMDN Term
Rigid endoscopic biopsy forceps, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.1075 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Rigid endoscopic biopsy forceps, single-use

Redpine 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 biopsy forceps, single-use.

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

Sources (1)

  • FDA UDI 3a45a72f-c2a7-4fff-a5ac-224d9178f1d4 32 fields · synced Jun 1, 2026