← Back to catalogue

Elmed

FDA UDI

Class I (US FDA UDI)

by Elmed Incorporated

Identity

Trade Name
ELMED FDA UDI
Generic Name
Test tube rack FDA UDI
Device Name
Aluminum Manifold-Single Rail Tube Holder, 0.196" Thick Anodized Clear Aluminum, 2" High x 8"Wide x 2" Deep. 9 Tubing Holder Sets of Varying sizes FDA UDI
Model / Reference
ST240220BC FDA UDI
Description
Aluminum Manifold-Single Rail Tube Holder, 0.196" Thick Anodized Clear Aluminum, 2" High x 8"Wide x 2" Deep. 9 Tubing Holder Sets of Varying sizes FDA UDI

Identifiers

Catalog Number
ST240220BC FDA UDI
Primary DI / UDI-DI
00842180197800 FDA UDI
FDA Product Code
LRP FDA UDI
GMDN Term
Test tube rack 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: Test tube rack

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

Similar devices

Also classified as Test tube rack.

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 8029e710-569c-4fac-afdc-695df1a38b30 35 fields · synced May 30, 2026