Identity
- Trade Name
- Large Tricycle FDA UDI
- Generic Name
- Assistive foot-propelled tricycle FDA UDI
- Device Name
- Adaptive Tricycle FDA UDI
- Model / Reference
- X340 FDA UDI
- Description
- Adaptive Tricycle FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00850001752282 FDA UDI
- FDA Product Code
- ION FDA UDI
- GMDN Term
- Assistive foot-propelled tricycle FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.5370 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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Assistive foot-propelled tricycle
Large Tricycle by Rifton Equipment — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Assistive foot-propelled tricycle.
- Small Tricycle — RIFTON EQUIPMENT · Class I
- Medium Tricycle — RIFTON EQUIPMENT · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Rifton Equipment
Sources (1)
- FDA UDI dd126e82-678f-4a0e-bf9a-9ed0c034e0e0 34 fields · synced May 30, 2026