Identity
- Trade Name
- Valmax FDA UDI
- Generic Name
- Manual traction wheelchair FDA UDI
- Model / Reference
- V16K2ADAELR FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00860013569846 FDA UDI
- 510(k) Number
- K231320 FDA UDI
- FDA Product Code
- IOR FDA UDI
- GMDN Term
- Manual traction wheelchair FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.3850 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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Manual traction wheelchair
Valmax by Supply Line Medical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Manual traction wheelchair.
- Valmax — Supply Line Medical · Class I
- Valmax — Supply Line Medical · Class I
- Valmax — Supply Line Medical · Class I
- Valmax — Supply Line Medical · Class I
- Valmax — Supply Line Medical · Class I
- Valmax — Supply Line Medical · Class I
Cleared under the same submission
K231320 also covers:
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Supply Line Medical
Sources (1)
- FDA UDI 689f4f53-054f-4c28-8642-df8199bc7c3c 33 fields · synced May 30, 2026