Identity
- Trade Name
- De Soutter Medical FDA UDI
- Generic Name
- Device sterilization/disinfection container, reusable FDA UDI
- Device Name
- 1/2 SIZE STERI-TRAY - 1 x MBC-709 - ASEPTIC FDA UDI
- Model / Reference
- 19300 FDA UDI
- Description
- 1/2 SIZE STERI-TRAY - 1 x MBC-709 - ASEPTIC FDA UDI
Identifiers
- Catalog Number
- 19300 FDA UDI
- Primary DI / UDI-DI
- 05051471164680 FDA UDI
- FDA Product Code
- GEY FDA UDI
- GMDN Term
- Device sterilization/disinfection container, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4820 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
Yes
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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Device sterilization/disinfection container, reusable
De Soutter Medical by De Soutter Medical, Ltd. — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- De Soutter Medical, Ltd.
Sources (1)
- FDA UDI e61e7fc6-0d44-47da-9511-b81eb872793e 34 fields · synced Jun 8, 2026