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Thermo Scientific Cryofuge 8

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 75007671

by Thermo Electron LED GmbH Zweigniederlassung Osterode

Identity

Trade Name
Thermo Scientific Cryofuge 8 EUDAMED
Thermo Scientific FDA UDI
Generic Name
Low-speed floor centrifuge, refrigerated FDA UDI
Device Name
Polaris MD EUDAMED
Heraeus Cryofuge 8, 200-240V, 50/60Hz FDA UDI
Model / Reference
75007671 EUDAMED
Heraeus Cryofuge 8 FDA UDI
Description
Heraeus Cryofuge 8, 200-240V, 50/60Hz FDA UDI

Identifiers

Catalog Number
75007671 FDA UDI
Primary DI / UDI-DI
10850685007057 EUDAMEDFDA UDI
Basic UDI-DI
0850685007750076_MDQH EUDAMED
Direct Marketing DI
10850685007057 EUDAMED
FDA Product Code
KSO FDA UDI
EMDN Code
B99 HAEMATOLOGY AND HAEMOTRANSFUSION DEVICES - OTHER EUDAMED
GMDN Term
Low-speed floor centrifuge, refrigerated FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
864.9275 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

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

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

Thermo Scientific Cryofuge 8 by Thermo Electron LED GmbH Zweigniederlassung Osterode — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID

Manufacturer's product page: Thermo Fisher Scientific Logo

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

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 f2e2fe4a-8345-4765-aeda-8d0ce1a8f4be 61 fields · synced Jul 9, 2026
  • FDA UDI f648239a-77d0-4f31-a517-c37a90c6ab23 35 fields · synced May 30, 2026