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Rotina 380

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 1706-01Model 1701, 1706

by Andreas Hettich GmbH & Co. KG

Identity

Trade Name
ROTINA 380 R, 110-127V 60Hz EUDAMED
ROTINA 380 FDA UDI
Generic Name
General-purpose centrifuge IVD FDA UDI
Device Name
ROTINA 380 / 380 R EUDAMED
Tabletop centrifuge, refrigerated FDA UDI
Model / Reference
1701, 1706 EUDAMED
1706-01 EUDAMED
ROTINA 380R - 100V-127V/50-60Hz FDA UDI
Description
Tabletop centrifuge, refrigerated FDA UDI

Identifiers

Catalog Number
1706-01 FDA UDI
Primary DI / UDI-DI
04050674037402 EUDAMEDFDA UDI
Basic UDI-DI
040506740100149T EUDAMED
Direct Marketing DI
04050674037402 EUDAMED
FDA Product Code
JQC FDA UDI
EMDN Code
W02069005 REFRIGERATED 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

Yes

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

Rotina 380 by Andreas Hettich GmbH & Co. KG — Class I — IVDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose centrifuge IVD.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

IVDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 0e94437a-2b54-4441-bba8-d0e2587b703a 34 fields · synced Jul 9, 2026
  • EUDAMED fda63343-9466-4b5a-930e-f97839e54e89 61 fields · synced Jul 9, 2026