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Thermo Scientific SL1 Plus-MD

EUDAMEDFDA UDI

Class A (EU MDR)

Ref 75009000

by Thermo Electron LED GmbH Zweigniederlassung Osterode

Identity

Trade Name
Thermo Scientific SL1 Plus-MD EUDAMED
Thermo Scientific FDA UDI
Generic Name
General-purpose centrifuge IVD FDA UDI
Device Name
GP1 Pro EUDAMED
SL1 Plus-MD 100-240V/ 50/60 Hz FDA UDI
Model / Reference
75009000 EUDAMED
SL1 Plus-MD FDA UDI
Description
SL1 Plus-MD 100-240V/ 50/60 Hz FDA UDI

Identifiers

Catalog Number
75009000 FDA UDI
Primary DI / UDI-DI
10850033408017 EUDAMEDFDA UDI
Basic UDI-DI
0850685007750092_IVD3Z EUDAMED
Direct Marketing DI
10850033408017 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 SL1 Plus-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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
DE-MF-000008786

Sources (2)

  • EUDAMED 3f8c458a-f51c-4e47-bd8c-fbc0cb3cc3d4 61 fields · synced Jul 15, 2026
  • FDA UDI d0edd503-c9b1-427f-a1ee-30ab5beb9e92 35 fields · synced May 30, 2026