Identity
- Trade Name
- Vyaire FDA UDI
- Generic Name
- Gas volume reference standard FDA UDI
- Device Name
- Calibration Syringe 3 L FDA UDI
- Model / Reference
- 720254 FDA UDI
- Description
- Calibration Syringe 3 L FDA UDI
Identifiers
- Catalog Number
- 720254 FDA UDI
- Primary DI / UDI-DI
- 34250892903928 FDA UDI
- FDA Product Code
- BXW FDA UDI
- GMDN Term
- Gas volume reference standard FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.1870 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
No
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Gas volume reference standard
Vyaire by Jaeger Medical GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Vyaire — Jaeger Medical GmbH · Class I
- Vyaire — Jaeger Medical GmbH · Class I
- Vyaire — Jaeger Medical GmbH · Class I
- Vyaire — Jaeger Medical GmbH · Class I
- Vyaire — Jaeger Medical GmbH · Class I
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
- Jaeger Medical GmbH
Sources (1)
- FDA UDI 2d3f9ef3-1124-4163-bf61-e62d29a22364 35 fields · synced Jun 8, 2026