← Back to catalogue

Foreign Body Retrieval Hood Protector

FDA UDI

Class II (US FDA UDI)

by Avanos Medical, Inc.

Identity

Trade Name
Foreign Body Retrieval Hood Protector FDA UDI
Generic Name
Medical device cleaning sponge/set FDA UDI
Device Name
Foreign Body Retrieval Hood Protector FDA UDI
Model / Reference
92810 FDA UDI
Description
Foreign Body Retrieval Hood Protector FDA UDI

Identifiers

Catalog Number
69392 FDA UDI
Primary DI / UDI-DI
00350770928104 FDA UDI
FDA Product Code
FED FDA UDI
GMDN Term
Medical device cleaning sponge/set 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

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Medical device cleaning sponge/set

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

Similar devices

Also classified as Medical device cleaning sponge/set.

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

Sources (1)

  • FDA UDI 6409a39d-20c8-4ca2-a314-33d4b025dd8f 35 fields · synced Jun 9, 2026