Identity
- Trade Name
- VYGON FDA UDI
- Generic Name
- Enteral tube extension, single-use FDA UDI
- Device Name
- Extension tube with clamp - Ø1.5x2.5mm - L.100cm FDA UDI
- Model / Reference
- 368.1071 FDA UDI
- Description
- Extension tube with clamp - Ø1.5x2.5mm - L.100cm FDA UDI
Identifiers
- Catalog Number
- 0003681071 FDA UDI
- Primary DI / UDI-DI
- 03660812113120 FDA UDI
- FDA Product Code
- FPD FDA UDI
- GMDN Term
- Enteral tube extension, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.5980 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: Enteral tube extension, single-use
Vygon by Vygon Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Vygon Corp.
Sources (1)
- FDA UDI eaf5066d-fa00-4f4c-9279-dacc8b893e3f 35 fields · synced Jun 8, 2026