Varilite Proform
by Cascade Designs, Inc. 60 variants
Part of a family of 60 devices: see the family page
Ref 76622
Varilite Proform (76622) is a Class I device made by Cascade Designs, Inc., registered in EUDAMED on 30 Sep 2026 (Basic UDI-DI 04081800030FN) and listed in FDA GUDID since 17 Aug 2023 (UDI-DI 00040818766224), active as of 24 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None, self-declared
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number04081800030FN 00040818766224 | Date30 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00040818766224 | Date17 Aug 2023 | StatusListed |
Official records
- EUDAMED public site 04081800030FN
- AccessGUDID record 00040818766224
Across registries
- EUDAMED Basic UDI-DI 04081800030FN registered 30 Sep 2026 Active
- FDA GUDID UDI-DI 00040818766224 listed 17 Aug 2023 Listed
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Timeline
- Listed FDA GUDID 00040818766224
- Registered EUDAMED 04081800030FN
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- ProFormNX, Dual, 16X16, INC EUDAMEDVarilite GUDID
- Generic name
- Air-filled chair cushion
- Device name
- VARILITE® ProForm NX™ Seating Systems
- Model / Ref / Catalog
- 76622, Proform
- Primary DI / UDI-DI
- 00040818766224
- Basic UDI-DI
- 04081800030FN
- FDA product code
- KIC
- EMDN code
- V08030102 Non-active anti-decubitus medical cushions
- GMDN term
- Air-filled chair cushion
- Device class
- Class I
- Regulation number
- 890.3175
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | 76622 | Proform |
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