Identity
- Trade Name
- VYAFUSER™ FDA UDI
- Generic Name
- Ambulatory syringe pump FDA UDI
- Device Name
- The VYAFUSER™ Pump is an ambulatory infusion pump intended for the subcutaneous delivery of VYALEV FDA UDI
- Model / Reference
- VYAFUSER PUMP KIT US/PR A FDA UDI
- Description
- The VYAFUSER™ Pump is an ambulatory infusion pump intended for the subcutaneous delivery of VYALEV FDA UDI
Identifiers
- Catalog Number
- 2089870410 FDA UDI
- Primary DI / UDI-DI
- 05713495000152 FDA UDI
- FDA Product Code
- FRN FDA UDI
- GMDN Term
- Ambulatory syringe pump FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5725 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
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
Yes
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
Dimensions & Sizes
- Size
- Length — 6.7 Inch FDA UDIWidth — 3 Inch FDA UDIDepth — 1.3 Inch FDA UDIWeight — 285 Gram FDA UDI
Category: Ambulatory syringe pump
Vyafuser™ by Phillips-Medisize A/S — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Ambulatory syringe pump.
- VYAFUSER™ — Phillips-Medisize A/S · 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
- Phillips-Medisize A/S
Sources (1)
- FDA UDI 22843d91-a8a9-4ad8-ac07-7ae0cd9cff45 37 fields · synced May 30, 2026