Identity
- Trade Name
- Automate 2500 Family FDA UDI
- Generic Name
- Specimen processing instrument IVD FDA UDI
- Device Name
- AutoMate1200 – Standard Sorter FDA UDI
- Model / Reference
- AutoMate 1200 FDA UDI
- Description
- AutoMate1200 – Standard Sorter FDA UDI
Identifiers
- Catalog Number
- ODL25120 FDA UDI
- Primary DI / UDI-DI
- 15099590364465 FDA UDI
- FDA Product Code
- JQP FDA UDI
- GMDN Term
- Specimen processing instrument IVD FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.2100 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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: Specimen processing instrument IVD
Automate 2500 Family by Beckman Coulter, Inc. — Class I — IVDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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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
- Beckman Coulter, Inc.
Sources (2)
- FDA UDI 3a7f35ea-ead2-45a8-8540-223e0574e29c 36 fields · synced Jun 18, 2026
- EUDAMED 1 fields · synced Jun 5, 2026