Globe Scientific

FDA UDI

Class I (US FDA UDI)

by Globe Scientific, Llc

Identity

Trade Name: Globe Scientific FDA UDI
Generic Name: Centrifuge tube IVD FDA UDI
Device Name: Tube, Urine Centrifuge, 12mL with Flared Top, PS, Kova Type, Graduated, 1000/Bag, 2 Bags/Unit FDA UDI
Model / Reference: 112015 FDA UDI
Description: Tube, Urine Centrifuge, 12mL with Flared Top, PS, Kova Type, Graduated, 1000/Bag, 2 Bags/Unit FDA UDI

Identifiers

Primary DI / UDI-DI: 00840095601160 FDA UDI
FDA Product Code: LXG 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

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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Centrifuge tube IVD

Globe Scientific by Globe Scientific, Llc — 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: Globe Scientific, Llc

Sources (1)

FDA UDI 034f6012-21a2-4466-91e8-c5a1bd3f5ca9 33 fields · synced May 31, 2026