← Back to catalogue

OSMETTE Sample Tube Rack, 50 ul

FDA UDI

Class I (US FDA UDI)

by Precision Systems, Inc.

Identity

Trade Name
OSMETTE Sample Tube Rack, 50 ul FDA UDI
Generic Name
Test tube rack FDA UDI
Device Name
OSMETTE Sample Tube Rack, 50 ul FDA UDI
Model / Reference
2044 FDA UDI
Description
OSMETTE Sample Tube Rack, 50 ul FDA UDI

Identifiers

Catalog Number
2044 FDA UDI
Primary DI / UDI-DI
00850041049441 FDA UDI
FDA Product Code
JJM FDA UDI
GMDN Term
Test tube rack FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2730 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

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Test tube rack

OSMETTE Sample Tube Rack, 50 ul by Precision Systems, Inc. — 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
Precision Systems, Inc.

Sources (1)

  • FDA UDI 7de4b41e-6708-4987-9f76-9770a93eab61 35 fields · synced May 30, 2026