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Elmed

FDA UDI

Class I (US FDA UDI)

by Elmed Incorporated

Identity

Trade Name
ELMED FDA UDI
Generic Name
Autopsy hand saw FDA UDI
Device Name
Stainless Steel Mayo Instrument Tray, 15" x 11" x 3/4" FDA UDI
Model / Reference
ST121022AK FDA UDI
Description
Stainless Steel Mayo Instrument Tray, 15" x 11" x 3/4" FDA UDI

Identifiers

Catalog Number
ST121022AK FDA UDI
Primary DI / UDI-DI
00842180190214 FDA UDI
FDA Product Code
LRP FDA UDI
GMDN Term
Autopsy hand saw 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: Autopsy hand saw

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Elmed Incorporated

Sources (1)

  • FDA UDI 10f181fa-1789-4e54-bf34-3c9f694f01fc 35 fields · synced May 31, 2026