Identity
- Trade Name
- Anti-Gravity Treadmill EUDAMEDAlterG Anti-Gravity Treadmill FDA UDI
- Generic Name
- Pneumatic-support treadmill FDA UDI
- Device Name
- AlterG Anti-Gravity Treadmill EUDAMEDThe Neo+ Anti-Gravity Treadmill is intended to be an entry-level product used in a clinical setting for standing, walking, or running in place for rehabilitation, or conditioning for individuals who may require or benefit from the use of body weight support FDA UDI
- Model / Reference
- Neo+ EUDAMEDFDA UDI
- Description
- The Neo+ Anti-Gravity Treadmill is intended to be an entry-level product used in a clinical setting for standing, walking, or running in place for rehabilitation, or conditioning for individuals who may require or benefit from the use of body weight support FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00850022788390 EUDAMEDFDA UDI
- Basic UDI-DI
- 0850022788Neo+3R EUDAMED
- Direct Marketing DI
- 00850022788390 EUDAMED
- FDA Product Code
- BXB FDA UDI
- EMDN Code
- Z129006 TREADMILLS FOR PHYSIOTHERAPY AND/OR DIAGNOSTIC USES EUDAMED
- GMDN Term
- Pneumatic-support treadmill FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 890.5380 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
Anti-Gravity Treadmill by Lifeward Ltd — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 0850022788Neo+3R | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Lifeward LTD.
- EUDAMED SRN
- IL-MF-000033442
- Authorised Representative
- Obelis s.a. BE-AR-000000106
Sources (2)
- EUDAMED 8dccbdba-8f31-4624-8950-6852ac804bd8 61 fields · synced May 30, 2026
- FDA UDI e5f0a638-86b8-4272-bc8f-103466847dd5 34 fields · synced May 30, 2026