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OSMETTE Sample Tubes, 0.2 ml, 12/pk

FDA UDI

Class I (US FDA UDI)

by Precision Systems, Inc.

Identity

Trade Name
OSMETTE Sample Tubes, 0.2 ml, 12/pk FDA UDI
Generic Name
General laboratory container, reusable FDA UDI
Device Name
OSMETTE Sample Tubes, 0.2 ml, 12/pk FDA UDI
Model / Reference
2022 FDA UDI
Description
OSMETTE Sample Tubes, 0.2 ml, 12/pk FDA UDI

Identifiers

Catalog Number
2022 FDA UDI
Primary DI / UDI-DI
00850041049229 FDA UDI
FDA Product Code
JJM FDA UDI
GMDN Term
General laboratory container, reusable 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: General laboratory container, reusable

OSMETTE Sample Tubes, 0.2 ml, 12/pk by Precision Systems, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General laboratory container, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Precision Systems, Inc.

Sources (1)

  • FDA UDI a1aac48e-6757-4531-8b72-5dfc06725d19 35 fields · synced Jun 6, 2026