e-motion®
GUDID 04046727211653
Alber GmbH
Wheelchair electric-motor-driven propulsion system| Primary Device ID | 04046727211653 |
| NIH Device Record Key | 8661ef69-6904-403d-aa18-07d71a9f4ca9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | e-motion® |
| Version Model Number | M25 |
| Company DUNS | 340348858 |
| Company Name | Alber GmbH |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | true |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04046727211653 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K192618
FDA Product Code
| ITI | Wheelchair, Powered |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-10-04 |
| Device Publish Date | 2022-09-26 |
On-Brand Devices [e-motion®]
Trademark Results [e-motion]
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.