Identity
- Trade Name
- BURT FDA UDI
- Generic Name
- Virtual-display rehabilitation system, powered-support, upper-limb FDA UDI
- Model / Reference
- M1200 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00867504000406 FDA UDI
- FDA Product Code
- IKK FDA UDI
- GMDN Term
- Virtual-display rehabilitation system, powered-support, upper-limb FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.1925 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
No
FDA UDI
Category: Virtual-display rehabilitation system, powered-support, upper-limb
Burt by Barrett Technology, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Virtual-display rehabilitation system, powered-support, upper-limb.
- Heaxel — HEALTH PIXEL SRL · Class II
- ®Fourier — Shanghai Fourier Intelligence Co., LTD · Class II
- InMotion ARM/HAND — BIONIK, INC. · Class II
- DIEGO — tyromotion GmbH · Class I
- Gloreha Active Package — IDROGENET SRL · Class I
- rebless planar — H ROBOTICS INC. · Class II
- REOGO — MOTORIKA MEDICAL (ISRAEL) LTD · Class II
- Gloreha Professional 2 — IDROGENET SRL · 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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Barrett Technology, Llc
Sources (1)
- FDA UDI 318ad505-1e4f-441b-bdf2-ab7f19700425 32 fields · synced Jun 6, 2026