Identity
- Trade Name
- SBH FDA UDI
- Generic Name
- Device sterilization/disinfection container, reusable FDA UDI
- Device Name
- Sterilization Container 1/1, Non Perforated Bottom, 585x274x96mm FDA UDI
- Model / Reference
- SB 106.100E Non Perforated Bottom FDA UDI
- Description
- Sterilization Container 1/1, Non Perforated Bottom, 585x274x96mm FDA UDI
Identifiers
- Catalog Number
- SB 106.100E FDA UDI
- Primary DI / UDI-DI
- 00850068304202 FDA UDI
- FDA Product Code
- KCT FDA UDI
- GMDN Term
- Device sterilization/disinfection container, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6850 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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dry Heat Sterilization FDA UDI
Category: Device sterilization/disinfection container, reusable
Sbh by SBH Surgical — 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
- SBH Surgical
Sources (1)
- FDA UDI 07bc43e9-f3e5-4d5f-a480-5f4a9b4db203 35 fields · synced Jun 1, 2026