Basic UDI-DI
Eu Mdd
Eu Md Class 2b
🇺🇸 United States
Allurion Practice Capsule
Code: B-FD013-09R3
Devices
1
Certificates
1
Notified Bodies
1
Auth. Representatives
2
Basic Information
- UDI-DI Code
- B-FD013-09R3
- Issuing Agency
- EUDAMED
- Device Model
- FD013-09
- Types
-
Implantable
- Regulation
- Eu Mdd Legacy
- Classification
- Eu Md Class 2b
- Manufacturer
- Allurion Technologies Inc.
- Last Updated
- June 17, 2024
Certificate Health
Total
1
Valid
0
Expiring < 6mo
0
Expired / Withdrawn
1
| Type | Number | Expiry Date | Status | |
|---|---|---|---|---|
| MDD Annex II (excluding section 4) | G1 003180 0006 | TÜV SÜD Product Service GmbH | May 26, 2024 |
Associated Devices
This Basic UDI-DI is associated with 1 device.
| Name | Status |
|---|---|
| Allurion Practice Capsule | On the market |