Identity
- Trade Name
- MIKRO 220 Robotic 200-240V/50-60Hz EUDAMEDMIKRO 200 Robotic FDA UDI
- Generic Name
- General-purpose centrifuge IVD FDA UDI
- Device Name
- MIKRO 220 Robotic EUDAMEDTabletop centrifuge, automated FDA UDI
- Model / Reference
- 2350 EUDAMEDMIKRO 220 Robotic 200-240V/50-60Hz FDA UDI
- Description
- Tabletop centrifuge, automated FDA UDI
Identifiers
- Catalog Number
- 2350 FDA UDI
- Primary DI / UDI-DI
- 04050674075916 EUDAMEDFDA UDI
- Basic UDI-DI
- 04050674010018A3 EUDAMED
- Direct Marketing DI
- 04050674075916 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 EUDAMEDClass 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
MIKRO 200 Robotic by Andreas Hettich GmbH & Co. KG — Class I — IVDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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Also classified as General-purpose centrifuge IVD.
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Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
IVDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | IVDR | — | Class I | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Andreas Hettich GmbH & Co. KG
Sources (2)
- FDA UDI 9451f5b7-7355-4848-8c74-252941dd4faa 34 fields · synced Jun 18, 2026
- EUDAMED b9d3c618-8044-4a01-9b85-7f58d0583643 61 fields · synced Jun 18, 2026