Basic UDI-DI
Eu Mdr
Eu Md Class 1
🇺🇸 United States
Aquaflex Gel Pad
Code: 085568300604000H8
Devices
3
Certificates
0
Notified Bodies
0
Auth. Representatives
1
Basic Information
- UDI-DI Code
- 085568300604000H8
- Issuing Agency
- GS1
- Device Model
- 04-02
- Types
- None provided
- Regulation
- Eu Mdr
- Classification
- Eu Md Class 1
- Manufacturer
- Parker Laboratories, Inc.
- Last Updated
- December 21, 2021
Certificate Health
No certificates associated with this Basic UDI-DI.
Associated Devices
This Basic UDI-DI is associated with 3 devices.
| Name | Status |
|---|---|
| Aquaflex Ultrasound Gel Pad | On the market |
| Aquaflex Ultrasound Gel Pad | On the market |
| Aquaflex Ultrasound Gel Pad | On the market |