← Back to catalogue

AHLGeneric

FDA UDI

Class II (US FDA UDI)

by Advanced Healthcare Ltd.

Identity

Trade Name
AHLGeneric FDA UDI
Generic Name
Gynaecological biopsy forceps, reusable FDA UDI
Device Name
Temporary Cavity Filling Material FDA UDI
Model / Reference
009X7 FDA UDI
Description
Temporary Cavity Filling Material FDA UDI

Identifiers

Primary DI / UDI-DI
05056009101236 FDA UDI
FDA Product Code
EMA FDA UDI
GMDN Term
Gynaecological biopsy forceps, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3275 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

Yes

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

Category: Gynaecological biopsy forceps, reusable

AHLGeneric by Advanced Healthcare Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gynaecological biopsy forceps, reusable.

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

Manufacturer
Advanced Healthcare Ltd.

Sources (1)

  • FDA UDI dfdfec90-fdf5-4cc9-afe5-dcff906bbbe5 34 fields · synced May 31, 2026