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Anrei

FDA UDI

Class II (US FDA UDI)

by Anrei Medical(HZ) Co., Ltd.

Identity

Trade Name
Anrei FDA UDI
Generic Name
Gastrointestinal endoscopic clip, long-term, non-bioabsorbable FDA UDI
Device Name
Single Use Rotatable and Repositionable Hemoclip FDA UDI
Model / Reference
HG-V-1C FDA UDI
Description
Single Use Rotatable and Repositionable Hemoclip FDA UDI

Identifiers

Primary DI / UDI-DI
06926839807686 FDA UDI
FDA Product Code
PKL FDA UDI
GMDN Term
Gastrointestinal endoscopic clip, long-term, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.4400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Gastrointestinal endoscopic clip, long-term, non-bioabsorbable

Anrei by Anrei Medical(HZ) Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gastrointestinal endoscopic clip, long-term, non-bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Anrei Medical(HZ) Co., Ltd.

Sources (1)

  • FDA UDI ec645ba7-1ae1-4a0a-b64c-55da98525856 33 fields · synced Jun 1, 2026