Single-Use Endoscopic Scissors

GUDID 06972520301650

Guangzhou Red Pine Medical Instrument Co., Ltd.

Rigid endoscopic scissors, single-use
Primary Device ID06972520301650
NIH Device Record Keyc2f3c103-8dcb-452c-8a1e-db76ea94158b
Commercial Distribution StatusIn Commercial Distribution
Brand NameSingle-Use Endoscopic Scissors
Version Model NumberRP-G-H01
Company DUNS417649868
Company NameGuangzhou Red Pine Medical Instrument Co., Ltd.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numbertrue
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS106972520301650 [Primary]

FDA Product Code

NWWHysteroscope Accessories

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-05-06
Device Publish Date2025-04-28

Devices Manufactured by Guangzhou Red Pine Medical Instrument Co., Ltd.

06972520301650 - Single-Use Endoscopic Scissors2025-05-06
06972520301650 - Single-Use Endoscopic Scissors2025-05-06
06972520300783 - REDPINE2024-09-10
06972520300790 - REDPINE2024-09-10
06972520301094 - REDPINE2024-09-10
06972520301100 - REDPINE2024-09-10
06972520301117 - REDPINE2024-09-10
06972520301124 - REDPINE2024-09-10
06972520301179 - REDPINE2024-09-10

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.