Clearview Disp Sample Tubes, 0.2 ml

FDA UDI

Class I (US FDA UDI)

by Precision Systems, Inc.

Identity

Trade Name: Clearview Disp Sample Tubes, 0.2 ml FDA UDI
Generic Name: General laboratory container, single-use FDA UDI
Device Name: Clearview Disp Sample Tubes, 0.2 ml, 500/pk FDA UDI
Model / Reference: 2028 FDA UDI
Description: Clearview Disp Sample Tubes, 0.2 ml, 500/pk FDA UDI

Identifiers

Catalog Number: 2028 FDA UDI
Primary DI / UDI-DI: 00850041049281 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

Clearview Disp Sample Tubes, 0.2 ml by Precision Systems, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General laboratory container, single-use.

CARDINAL HEALTH — Cardinal Health 200, LLC · Class I
Marketlab — MARKETLAB INC. · Class I
CARDINAL HEALTH — Cardinal Health 200, LLC · Class I
Vial Set — Argon Medical Devices, Inc. · Class I
KBMED — KB Medical (group), Inc. · Class I
Gongdong — Zhejiang Gongdong Medical Technology Co., Ltd., · Class I
Gongdong — Zhejiang Gongdong Medical Technology Co., Ltd., · Class I
KBMED — KB Medical (group), Inc. · Class I

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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Precision Systems, Inc.

Sources (1)

FDA UDI be7aaa01-5897-4deb-a13b-f98c15a43216 35 fields · synced May 30, 2026