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LabChoice Microcentrifuge Tubes, Polypropylene, 5mL, Sterile

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
LabChoice Microcentrifuge Tubes, Polypropylene, 5mL, Sterile FDA UDI
Generic Name
Centrifuge tube IVD FDA UDI
Device Name
Features: Snap cap, Graduation marks, Frosted writing area, RCF 15,000xg, STERILE FDA UDI
Model / Reference
42123 FDA UDI
Description
Features: Snap cap, Graduation marks, Frosted writing area, RCF 15,000xg, STERILE FDA UDI

Identifiers

Primary DI / UDI-DI
00840117337299 FDA UDI
FDA Product Code
JQC FDA UDI
GMDN Term
Centrifuge tube IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Centrifuge tube IVD

LabChoice Microcentrifuge Tubes, Polypropylene, 5mL, Sterile by Dynarex Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Centrifuge tube IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI 2d3a4e56-4c1d-4e82-a0a6-fbfb6405eebf 33 fields · synced May 30, 2026