Identity
- Trade Name
- Backcheck Valve FDA UDI
- Generic Name
- In-line backflow valve, single-use FDA UDI
- Device Name
- Normally Closed Check Valve FDA UDI
- Model / Reference
- 415062 FDA UDI
- Description
- Normally Closed Check Valve FDA UDI
Identifiers
- Catalog Number
- 415062 FDA UDI
- Primary DI / UDI-DI
- 04022495238337 FDA UDI
- FDA Product Code
- FPA FDA UDI
- GMDN Term
- In-line backflow valve, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5440 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: In-line backflow valve, single-use
Backcheck Valve by B. Braun Medical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as In-line backflow valve, single-use.
- ICU Medical — ICU MEDICAL, INC. · Class II
- Medex — ICU MEDICAL, INC. · Class II
- ICU Medical — ICU MEDICAL, INC. · Class II
- Medex — ICU MEDICAL, INC. · Class II
- Cook — COOK INCORPORATED · Class II
- ICU Medical — ICU MEDICAL, INC. · Class II
- PEAK MEDICAL — PEAK MEDICAL Distribution Inc · Class II
- ICU Medical — ICU MEDICAL, INC. · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- B. Braun Medical Inc.
Sources (1)
- FDA UDI 9110d4a9-49b2-47ce-936f-cacfda148815 35 fields · synced May 31, 2026