Identity
- Trade Name
- SBH FDA UDI
- Generic Name
- Device sterilization/disinfection container, reusable FDA UDI
- Device Name
- 1/1, Sterilization Container Perforated Lid, Blue, 585mm x 278mm, 23" x 11" FDA UDI
- Model / Reference
- K123234 FDA UDI
- Description
- 1/1, Sterilization Container Perforated Lid, Blue, 585mm x 278mm, 23" x 11" FDA UDI
Identifiers
- Catalog Number
- SB 100.040E FDA UDI
- Primary DI / UDI-DI
- 00850068304011 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
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
MR Unsafe 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 875c86e0-90e3-4f77-8689-0dac150c32c4 35 fields · synced May 30, 2026