Anrei

GUDID 06926839809147

Single Use Injection Needle

Anrei Medical(HZ) Co.,Ltd.

Sclerotherapy endoscopic needle, single-use
Primary Device ID06926839809147
NIH Device Record Key17881394-0fcc-4a88-b771-c2a65a1584a9
Commercial Distribution StatusIn Commercial Distribution
Brand NameAnrei
Version Model NumberNE-C2508
Company DUNS529128653
Company NameAnrei Medical(HZ) Co.,Ltd.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numbertrue
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS106926839809147 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FBKEndoscopic Injection Needle, Gastroenterology-Urology

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-01-16
Device Publish Date2025-01-08

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26948318968828M00515101
16948318903921M00515100
06926839806078Single-use Biopsy Foreps
06926839806061Single-use Biopsy Foreps
06926839806054Single-use Biopsy Foreps
06926839806047Single-use Biopsy Foreps
06926839806030Single-use Biopsy Foreps
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06926839800588Single-use Biopsy Forceps
06926839800571Single-use Biopsy Forceps
06926839809147Single Use Injection Needle

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