Identity
- Trade Name
- AVANTI FDA UDI
- Generic Name
- Haemostasis valve FDA UDI
- Device Name
- SI AVANTI+ PED .035 F5 W/O GW FDA UDI
- Model / Reference
- 402605R FDA UDI
- Description
- SI AVANTI+ PED .035 F5 W/O GW FDA UDI
Identifiers
- Catalog Number
- 402605R FDA UDI
- Primary DI / UDI-DI
- 10705032000550 FDA UDI
- FDA Product Code
- DRE FDA UDI
- GMDN Term
- Haemostasis valve FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1310 FDA UDI
- 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
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Avanti by Cordis Corp. — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Cordis Corp.
Sources (1)
- FDA UDI 189b99aa-5aa3-4072-a3ad-af81a7c30874 35 fields · synced May 31, 2026