Identity
- Trade Name
- Celerity FDA UDI
- Generic Name
- Biological sterilization indicator FDA UDI
- Device Name
- The Celerity 20 STEAM Process Challenge Device for Gravity Cycles is for routine monitoring, qualification testing, load monitoring and product testing in for gravity cycles. It has 25 packs with 25 controls. FDA UDI
- Model / Reference
- LCB050 FDA UDI
- Description
- The Celerity 20 STEAM Process Challenge Device for Gravity Cycles is for routine monitoring, qualification testing, load monitoring and product testing in for gravity cycles. It has 25 packs with 25 controls. FDA UDI
Identifiers
- Catalog Number
- LCB050 FDA UDI
- Primary DI / UDI-DI
- 10724995161573 FDA UDI
- FDA Product Code
- FRC FDA UDI
- GMDN Term
- Biological sterilization indicator 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
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Biological sterilization indicator
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 b585cf89-2af7-4341-92d6-2416b5706de2 35 fields · synced Jun 8, 2026