Identity
- Trade Name
- BAHADIR USA FDA UDI
- Generic Name
- Device sterilization/disinfection container, reusable FDA UDI
- Device Name
- CONTAINER WIDE BODY BOTTOM PERFORATED - SILVER 600X400X120MM FDA UDI
- Model / Reference
- Y 111.62W FDA UDI
- Description
- CONTAINER WIDE BODY BOTTOM PERFORATED - SILVER 600X400X120MM FDA UDI
Identifiers
- Primary DI / UDI-DI
- B060Y11162W17 FDA UDI
- 510(k) Number
- K131407 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
Single Use
No
Implantable
No
Contains Latex
No
Prescription Use
No
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
No
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
No
Manufacturing Date
No
Category: Device sterilization/disinfection container, reusable
Bahadir USA Sterilization Wrap Containers, Trays, Cassettes & Other Accessories are designed to provide a safe and efficient way to sterilize and disinfect medical devices. These reusable containers feature a durable silver finish and are suitable for use in a variety of settings, including hospitals and clinics. With their compact design and easy-to-use features, Bahadir USA Sterilization Wrap Containers make it easier to maintain high standards of infection control and patient safety.
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Cleared under the same submission
K131407 also covers:
- BAHADIR USA — BAHADIR USA LLC
- BAHADIR USA — BAHADIR USA LLC
- BAHADIR USA — BAHADIR USA LLC
- BAHADIR USA — BAHADIR USA LLC
- BAHADIR USA — BAHADIR USA LLC
- BAHADIR USA — BAHADIR USA LLC
- BAHADIR USA — BAHADIR USA LLC
- BAHADIR USA — BAHADIR USA LLC
- BAHADIR USA — BAHADIR USA LLC
- BAHADIR USA — BAHADIR USA LLC
- BAHADIR USA — BAHADIR USA LLC
- BAHADIR USA — BAHADIR USA LLC
Authorization Coverage (1 country)
Regulatory Authorizations
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Bahadir Usa Llc
Sources (1)
- FDA UDI d621457a-3317-4f33-a240-b8d04ebc327f 35 fields · synced Jul 17, 2026