Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- Device sterilization/disinfection container, reusable FDA UDI
- Device Name
- GENESIS FULL-LENGTH CONTAINER 23 X 12 inches58.4 X 30.5CM 4 inches10.2CM DEEP PERFORATED BOTTOM, PURPLE FDA UDI
- Model / Reference
- CD3-4B-PURPLE FDA UDI
- Description
- GENESIS FULL-LENGTH CONTAINER 23 X 12 inches58.4 X 30.5CM 4 inches10.2CM DEEP PERFORATED BOTTOM, PURPLE FDA UDI
Identifiers
- Catalog Number
- CD34BPURPLE FDA UDI
- Primary DI / UDI-DI
- 10885403195068 FDA UDI
- 510(k) Number
- K142529 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
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Device sterilization/disinfection container, reusable
V. Mueller by Steris Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K142529 also covers:
- V. Mueller — STERIS CORPORATION
- V. Mueller — STERIS CORPORATION
- V. Mueller — STERIS CORPORATION
- V. Mueller — STERIS CORPORATION
- V. Mueller — STERIS CORPORATION
- V. Mueller — STERIS CORPORATION
- V. Mueller — STERIS CORPORATION
- V. Mueller — STERIS CORPORATION
- V. Mueller — STERIS CORPORATION
- V. Mueller — STERIS CORPORATION
- V. Mueller — STERIS CORPORATION
- V. Mueller — STERIS CORPORATION
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Steris Corporation
Sources (1)
- FDA UDI fa5a4d71-9585-4cb5-baf2-cd72a2b54c59 36 fields · synced Jun 8, 2026