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Thermo Scientific Multifuge X1 Pro-MD

EUDAMEDFDA UDI

Class A (EU MDR)

Ref 75009210

by Thermo Electron LED GmbH Zweigniederlassung Osterode

Identity

Trade Name
Thermo Scientific Multifuge X1 Pro-MD EUDAMED
Thermo Scientific FDA UDI
Generic Name
General-purpose centrifuge IVD FDA UDI
Device Name
GP1 Pro EUDAMED
Multifuge X1 Pro-MD 100-240V/ 50/60 Hz FDA UDI
Model / Reference
75009210 EUDAMED
Multifuge X1 Pro-MD FDA UDI
Description
Multifuge X1 Pro-MD 100-240V/ 50/60 Hz FDA UDI

Identifiers

Catalog Number
75009210 FDA UDI
Primary DI / UDI-DI
10850033408048 EUDAMEDFDA UDI
Basic UDI-DI
0850685007750092_IVD3Z EUDAMED
Direct Marketing DI
10850033408048 EUDAMED
FDA Product Code
JQC FDA UDI
EMDN Code
W02069003 CENTRIFUGES EUDAMED
GMDN Term
General-purpose centrifuge IVD FDA UDI

Classification

Device Class
Class A EUDAMED
Class I FDA UDI
Regulation Number
862.2050 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

No

EUDAMED

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

Yes

FDA UDI

Category: General-purpose centrifuge IVD

Thermo Scientific Multifuge X1 Pro-MD by Thermo Electron LED GmbH Zweigniederlassung Osterode — Class A — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID

Similar devices

Also classified as General-purpose centrifuge IVD.

Manufacturer's product page: Thermo Fisher Scientific Logo

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
DE-MF-000008786

Sources (2)

  • EUDAMED b4b3d346-8301-41cc-b419-e947e58775b0 61 fields · synced Jun 19, 2026
  • FDA UDI bc92389b-ba65-4e7d-ad9e-2ec234863461 35 fields · synced May 30, 2026