Doppler Flow Wire Cover DFC101
by Advance Medical Designs, Inc.
Ref DFC-101
Doppler Flow Wire Cover DFC101 is a device classified as Class I in the EU and Class II in the US made by Advance Medical Designs, Inc., registered in EUDAMED on 2 Nov 2026 (Basic UDI-DI 84834000DFC-1012X), cleared under FDA 510(k) K850959 on 9 Apr 1985 and listed in FDA GUDID since 13 Mar 2024 (UDI-DI 00848340002366), active as of 7 Nov 2026. One FDA recall is linked to it.
Active
Valid until
No date given
FDA recalls
None ongoingTrust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number84834000DFC-1012X 00848340002366 | Date2 Nov 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00848340002366 | Date13 Mar 2024 | StatusListed |
| United States | FDA 510(k)SESE GUDID | NumberK850959 | Date9 Apr 1985 | StatusActive |
Official records
- EUDAMED public site 84834000DFC-1012X
- AccessGUDID record 00848340002366
- FDA 510(k) database K850959
Across registries
- EUDAMED Basic UDI-DI 84834000DFC-1012X registered 2 Nov 2026 Active
- FDA 510(k) K850959 decided 9 Apr 1985 Active
- FDA GUDID UDI-DI 00848340002366 listed 13 Mar 2024 Listed
Recalls
-
- Terminated Z-1036-04
The product may come apart when excessive force is applied to the coupler.
Timeline
- Cleared FDA 510(k) K850959
- Recall initiated FDA recalls Z-1036-04
- Listed FDA GUDID 00848340002366
- Registered EUDAMED 84834000DFC-1012X
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Doppler Flow Wire Cover
- Generic name
- Medical equipment/instrument drape, single-use
- Model / reference
- DFC-101 EUDAMEDDFC101 GUDID
- Primary DI / UDI-DI
- 00848340002366
- Basic UDI-DI
- 84834000DFC-1012X
- 510(k) Number
- FDA product code
- JAA
- EMDN code
- T030199 Covers, instruments and equipment - other
- GMDN term
- Medical equipment/instrument drape, single-use
- Device class
- Class I EUDAMEDClass II GUDID
- Regulation number
- 892.1650
- EU registration type
- Standard device
- EU market of registration
- France
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Ethylene Oxide
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | DFC-101 | DFC101 |
| Device class | Class I | Class II |
| Supplied sterile | Yes | No |
| Sterilise before use | No | Yes |
Registry differences
EUDAMED and FDA GUDID describe the same product (same UDI-DI) and state different values:
- Supplied sterile UDI-DI 00848340002366: EUDAMED states Yes, FDA GUDID states No.
- Sterilise before use UDI-DI 00848340002366: EUDAMED states No, FDA GUDID states Yes.
Device class is stated on each registry's own scale: Class I in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.
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