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Globe Scientific

FDA UDI

Class I (US FDA UDI)

by Globe Scientific, Llc

Identity

Trade Name
Globe Scientific FDA UDI
Generic Name
General-purpose centrifuge IVD FDA UDI
Device Name
Centrifuge, Clinical, Multi-Purpose, 120V, 60Hz, US Plug (Rotor Not Included) FDA UDI
Model / Reference
GCC-MP FDA UDI
Description
Centrifuge, Clinical, Multi-Purpose, 120V, 60Hz, US Plug (Rotor Not Included) FDA UDI

Identifiers

Primary DI / UDI-DI
00840095655484 FDA UDI
FDA Product Code
JQC FDA UDI
GMDN Term
General-purpose centrifuge 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

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General-purpose centrifuge IVD

Globe Scientific by Globe Scientific, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose centrifuge IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1f092643-84a4-4765-8592-9f7edda5fdd8 33 fields · synced Jun 8, 2026