← Back to catalogue

Elmed

FDA UDI

Class I (US FDA UDI)

by Elmed Incorporated

Identity

Trade Name
ELMED FDA UDI
Generic Name
Surgical mallet FDA UDI
Device Name
Mallet 8” Overall Length, Handle Length 4.5”, Head Weight 1.75lb, Head diameter 1.5” with Black Teflon Handle FDA UDI
Model / Reference
23-7815 FDA UDI
Description
Mallet 8” Overall Length, Handle Length 4.5”, Head Weight 1.75lb, Head diameter 1.5” with Black Teflon Handle FDA UDI

Identifiers

Catalog Number
23-7815 FDA UDI
Primary DI / UDI-DI
00842180159471 FDA UDI
FDA Product Code
GFJ FDA UDI
GMDN Term
Surgical mallet 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: Surgical mallet

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

Similar devices

Also classified as Surgical mallet.

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
Elmed Incorporated

Sources (1)

  • FDA UDI c9ed9a7d-e85d-4a41-b35a-79c030fce938 35 fields · synced May 30, 2026