Identity
- Trade Name
- V. Mueller FDA UDI
- Generic Name
- Cyclodialysis cannula FDA UDI
- Device Name
- V. Mueller SHEETS CANNULA SPATULA TIP WITH FRONT AND SIDE PORTS 19 GAUGE FDA UDI
- Model / Reference
- OP0901-201 FDA UDI
- Description
- V. Mueller SHEETS CANNULA SPATULA TIP WITH FRONT AND SIDE PORTS 19 GAUGE FDA UDI
Identifiers
- Catalog Number
- OP0901-201 FDA UDI
- Primary DI / UDI-DI
- 10885403089473 FDA UDI
- FDA Product Code
- HND FDA UDI
- GMDN Term
- Cyclodialysis cannula FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.4350 FDA UDI
- Commercial Distribution
- Not 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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
V. Mueller by Carefusion 2200, Inc. — Class I — 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 | Class I | Pending data |
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Manufacturer
- Manufacturer
- Carefusion 2200, Inc.
Sources (1)
- FDA UDI b2eb79e5-78db-4a68-a6bd-2254c8f7b2e2 36 fields · synced Sep 18, 2026