Identity
- Trade Name
- STERIDENT FDA UDI
- Generic Name
- Dry-heat sterilizer FDA UDI
- Device Name
- STERIDENT 230V MODEL FDA UDI
- Model / Reference
- 200 FDA UDI
- Description
- STERIDENT 230V MODEL FDA UDI
Identifiers
- Primary DI / UDI-DI
- B234KMHSD201000230 FDA UDI
- FDA Product Code
- KMH FDA UDI
- GMDN Term
- Dry-heat sterilizer FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6870 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
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: Dry-heat sterilizer
Sterident by CPAC Equipment, Inc. — 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
- CPAC Equipment, Inc.
Sources (1)
- FDA UDI 2bdc1831-3638-42de-ac63-3fd1d59cc8c1 33 fields · synced Jun 1, 2026