Identity
- Trade Name
- cobas i 601 SBL FDA UDI
- Generic Name
- Liquid chromatography/mass spectrometry (LC/MS) analyser IVD FDA UDI
- Model / Reference
- 10271574001 FDA UDI
Identifiers
- Catalog Number
- 10271574001 FDA UDI
- Primary DI / UDI-DI
- 07613336231357 FDA UDI
- FDA Product Code
- DOP FDA UDI
- GMDN Term
- Liquid chromatography/mass spectrometry (LC/MS) analyser IVD FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.2860 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
Yes
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
No
FDA UDI
Category: Liquid chromatography/mass spectrometry (LC/MS) analyser IVD
cobas i 601 SBL by Roche Diagnostics Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- cobas i 601 — Roche Diagnostics Corp. · Class I
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Roche Diagnostics Corp.
Sources (1)
- FDA UDI 511c4b10-ab12-413b-adc5-1ea06dab4eb0 33 fields · synced May 30, 2026