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Elmed

FDA UDI

Class I (US FDA UDI)

by Elmed Incorporated

Identity

Trade Name
ELMED FDA UDI
Generic Name
Dissection board FDA UDI
Device Name
Teflon-Custom Size Cartilage Cutting Board, 3"L x 5”W x 5/8”H. FDA UDI
Model / Reference
01-2242 FDA UDI
Description
Teflon-Custom Size Cartilage Cutting Board, 3"L x 5”W x 5/8”H. FDA UDI

Identifiers

Catalog Number
01-2242 FDA UDI
Primary DI / UDI-DI
00842180167179 FDA UDI
FDA Product Code
GEN FDA UDI
GMDN Term
Dissection board FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

No

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dissection board

Elmed by Elmed Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dissection board.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Elmed Incorporated

Sources (1)

  • FDA UDI 1c36f72e-8d85-4cca-a692-b88b14ac63ff 35 fields · synced May 30, 2026