OSMETTE Sample Tubes, 30 ul

FDA UDI

Class I (US FDA UDI)

by Precision Systems, Inc.

Identity

Trade Name: OSMETTE Sample Tubes, 30 ul FDA UDI
Generic Name: General laboratory container, single-use FDA UDI
Device Name: OSMETTE Sample Tubes, 30 ul, 1000/pk FDA UDI
Model / Reference: 2020 FDA UDI
Description: OSMETTE Sample Tubes, 30 ul, 1000/pk FDA UDI

Identifiers

Catalog Number: 2020 FDA UDI
Primary DI / UDI-DI: 00850041049533 FDA UDI
FDA Product Code: JJM FDA UDI
GMDN Term: General laboratory container, single-use 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: General laboratory container, single-use

OSMETTE Sample Tubes, 30 ul by Precision Systems, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Precision Systems, Inc.

Sources (1)

FDA UDI 0257dc64-609b-42a0-ac54-396dfa905dd5 35 fields · synced May 30, 2026