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LabChoice Centrifuge Tubes, Polypropylene, 50 ML

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
LabChoice Centrifuge Tubes, Polypropylene, 50 ML FDA UDI
Generic Name
Centrifuge tube IVD FDA UDI
Device Name
Features: Transparent, flap caps, printed graduation, white writing area, RCF 12, 000xg, Self-Standing FDA UDI
Model / Reference
42104 FDA UDI
Description
Features: Transparent, flap caps, printed graduation, white writing area, RCF 12, 000xg, Self-Standing FDA UDI

Identifiers

Primary DI / UDI-DI
00840117338203 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Centrifuge tube IVD

LabChoice Centrifuge Tubes, Polypropylene, 50 ML 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 78e889fb-956b-4eb9-9bbd-c5893f0b1bac 33 fields · synced May 30, 2026