Identity
- Trade Name
- SectionStar FDA UDI
- Generic Name
- Rotary microtome IVD FDA UDI
- Model / Reference
- 810-00001 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00198168976302 FDA UDI
- FDA Product Code
- IDO FDA UDI
- GMDN Term
- Rotary microtome IVD FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 864.3010 FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
SectionStar by Clarapath, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Clarapath, Inc.
Sources (1)
- FDA UDI 0f0c3e30-4811-486d-ba02-f3a094539d1f 33 fields · synced Jun 1, 2026