← Back to catalogue

Sharn Inc

FDA UDI

Class I (US FDA UDI)

by Sharn Anesthesia

Identity

Trade Name
Sharn Inc FDA UDI
Generic Name
Endoscopic bite block, basic, single-use FDA UDI
Device Name
Soft BiteBlock, Medium, Individually Wrapped PK100 FDA UDI
Model / Reference
35397 FDA UDI
Description
Soft BiteBlock, Medium, Individually Wrapped PK100 FDA UDI

Identifiers

Catalog Number
35397 FDA UDI
Primary DI / UDI-DI
00817518021355 FDA UDI
FDA Product Code
MNK FDA UDI
GMDN Term
Endoscopic bite block, basic, single-use 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

No

FDA UDI

Category: Endoscopic bite block, basic, single-use

Sharn Inc by Sharn Anesthesia — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic bite block, basic, single-use.

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
Sharn Anesthesia

Sources (1)

  • FDA UDI 3e394ce8-0c59-4a7d-b56e-759c80442736 35 fields · synced May 31, 2026