Identity
- Trade Name
- AVANTI FDA UDI
- Generic Name
- Haemostasis valve FDA UDI
- Device Name
- AVANTI + 4F STD W/GW FDA UDI
- Model / Reference
- 504604X FDA UDI
- Description
- AVANTI + 4F STD W/GW FDA UDI
Identifiers
- Catalog Number
- 504604X FDA UDI
- Primary DI / UDI-DI
- 10705032009935 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
- 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
Category: Haemostasis valve
Avanti by Cordis US Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- AVANTI — Cordis Corp. · Class II
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 US Corp.
Sources (1)
- FDA UDI 76edb265-156e-4f69-88c1-6e2d29b271a2 35 fields · synced May 31, 2026