Identity
- Trade Name
- Celerity FDA UDI
- Generic Name
- Test tube heater FDA UDI
- Device Name
- The Celerity HP Incubator was designed exclusively to incubate and read activated Celerity 20 HP Biological Indicators. FDA UDI
- Model / Reference
- Incubator FDA UDI
- Description
- The Celerity HP Incubator was designed exclusively to incubate and read activated Celerity 20 HP Biological Indicators. FDA UDI
Identifiers
- Catalog Number
- LCB046 FDA UDI
- Primary DI / UDI-DI
- 00724995201845 FDA UDI
- FDA Product Code
- FRC FDA UDI
- GMDN Term
- Test tube heater FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.2800 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
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Test tube heater
Celerity by Steris Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 II | Pending data |
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Manufacturer
- Manufacturer
- Steris Corporation
Sources (1)
- FDA UDI f4bb73a1-cd17-4b2b-9bdc-9603972c73a8 36 fields · synced Jun 6, 2026