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Foreign Body Grasping Forceps

FDA UDI

Class II (US FDA UDI)

by Avanos Medical, Inc.

Identity

Trade Name
Foreign Body Grasping Forceps FDA UDI
Generic Name
Flexible endoscopic stone-retrieval forceps, single-use FDA UDI
Device Name
Foreign Body Grasping Forceps FDA UDI
Model / Reference
92762 FDA UDI
Description
Foreign Body Grasping Forceps FDA UDI

Identifiers

Catalog Number
60622 FDA UDI
Primary DI / UDI-DI
00350770927626 FDA UDI
FDA Product Code
OCZ FDA UDI
GMDN Term
Flexible endoscopic stone-retrieval forceps, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

Yes

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

Yes

FDA UDI

Category: Flexible endoscopic stone-retrieval forceps, single-use

Foreign Body Grasping Forceps by Avanos Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible endoscopic stone-retrieval forceps, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Avanos Medical, Inc.

Sources (1)

  • FDA UDI ac3209c8-0f8b-4168-a6c6-e55d431c6e0d 35 fields · synced Jun 9, 2026