FDA UDI
In Commercial Distribution
🇺🇸 United States
Andago
DI: 07640174660230
·
Model: V2.0
·
HOCOMA AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
Basic Information
- Brand Name
- Andago
- Primary DI
- 07640174660230
- Version / Model
- V2.0
- Catalog Number
- 31585
- Company Name
- HOCOMA AG
- Labeler DUNS
- 487876203
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2016-08-22
- Public Version
- 2
- Public Version Date
- 2018-03-29
- Public Version Status
- Update
- Public Device Record Key
- f3040203-6df6-4a12-b87d-94dc416a01d2
Device Characteristics
- Single Use
- No
- Prescription Use (Rx)
- Yes
- Over the Counter (OTC)
- No
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- No
- MRI Safety
- Labeling does not contain MRI Safety Information
- Direct Marking Exempt
- No
- PM Exempt
- Yes
- Has Serial Number
- Yes
- Has Lot/Batch Number
- No
- Has Manufacturing Date
- Yes
- Has Expiration Date
- No
- Has Donation ID
- No
Sterilization
- Is Sterile
- No
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| BXB | Exerciser, Powered | Physical Medicine | 890.5380 | 1 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 61942 | Mobile gait rehabilitation system, harness-support | A mobile assembly of battery-powered devices designed to assist a patient with a walking/balance disability (neurological, muscular, cardiovascular, or orthopaedic in origin) to regain lost motor function, by enabling the patient to walk over ground (i.e., not on a treadmill) whilst supported from above. It consists of a mobile rigid framework on electronically-controlled wheels, a patient harness with suspension assembly, and motion sensors; the device senses patient movements and automatically follows the patient. The patient is supported overhead to assist rehabilitation and provide fall protection. It is intended to be used in a clinical setting under professional supervision. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 07640174660230 | GS1 |