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Medco Manufacturing

FDA UDI

Class I (US FDA UDI)

by Medco Manufacturing LLC

Identity

Trade Name
Medco Manufacturing FDA UDI
Generic Name
Test tube rack FDA UDI
Device Name
Polypropylene Syringe Rack: M/L, Holds 24 20cc-60cc Volume Syringes FDA UDI
Model / Reference
SR20-ML FDA UDI
Description
Polypropylene Syringe Rack: M/L, Holds 24 20cc-60cc Volume Syringes FDA UDI

Identifiers

Primary DI / UDI-DI
00810130452217 FDA UDI
FDA Product Code
MDM 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Test tube rack

Medco Manufacturing by Medco Manufacturing LLC — 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

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Manufacturer

Manufacturer
Medco Manufacturing LLC

Sources (1)

  • FDA UDI 206def8e-f185-4ad7-a6cf-a74641e8d010 34 fields · synced May 30, 2026