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Sharn Inc

FDA UDI

Class I (US FDA UDI)

by Sharn Anesthesia

Identity

Trade Name
Sharn Inc FDA UDI
Generic Name
Medical device cleaning sponge/set FDA UDI
Device Name
Safe-Soak Endo Sponge Tubular Sponge/Dispenser Box PK25 FDA UDI
Model / Reference
41486 FDA UDI
Description
Safe-Soak Endo Sponge Tubular Sponge/Dispenser Box PK25 FDA UDI

Identifiers

Catalog Number
41486 FDA UDI
Primary DI / UDI-DI
00817518021379 FDA UDI
FDA Product Code
MNL FDA UDI
GMDN Term
Medical device cleaning sponge/set FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.1500 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

No

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

Yes

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

Sharn Inc by Sharn Anesthesia — Class I — 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

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Manufacturer

Manufacturer
Sharn Anesthesia

Sources (1)

  • FDA UDI f9076500-ba08-4dbc-b247-0461a14297f2 35 fields · synced May 30, 2026