Identity
- Trade Name
- MABIS DMI FDA UDI
- Generic Name
- Obstetrical/gynaecological surgical procedure kit, non-medicated, single-use FDA UDI
- Device Name
- OB KIT - CANADIAN STYLE FDA UDI
- Model / Reference
- 650-4009-0000 FDA UDI
- Description
- OB KIT - CANADIAN STYLE FDA UDI
Identifiers
- Catalog Number
- 650-4009-0000 FDA UDI
- Primary DI / UDI-DI
- 00041298400905 FDA UDI
- GMDN Term
- Obstetrical/gynaecological surgical procedure kit, non-medicated, single-use FDA UDI
Classification
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Mabis Dmi by Dms Holdings, Inc., — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Dms Holdings, Inc.,
Sources (1)
- FDA UDI 2e3fc8ef-4e92-408e-85ca-6ebeefbe81f5 35 fields · synced Jun 6, 2026