Bridge Dressing Kit XF-BDMF1
by Genadyne Biotechnologies Inc.
Ref XF-BKMF1
Bridge Dressing Kit XF-BDMF1 is a medical device (EU MDD Class IIb; FDA Class II; FDA product code OMP, Negative Pressure Wound Therapy Powered Suction Pump; EMDN category polyurethane dressings) made by Genadyne Biotechnologies Inc., registered in EUDAMED on 12 Jun 2026 (Basic UDI-DI B-00849405023104), cleared under FDA 510(k) K092992 on 29 Jun 2010 and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00849405023104), active as of 24 Oct 2026.
Active
Valid until
No date given
FDA recalls
None found
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD EUDAMED | NumberB-00849405023104 00849405023104 | Date12 Jun 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00849405023104 | Date24 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE GUDID | NumberK092992 | Date29 Jun 2010 | StatusActive |
Official records
- EUDAMED public site B-00849405023104
- AccessGUDID record 00849405023104
- FDA 510(k) database K092992
Across registries
- EUDAMED Basic UDI-DI B-00849405023104 registered 12 Jun 2026 Active
- FDA 510(k) K092992 decided 29 Jun 2010 Active
- FDA GUDID UDI-DI 00849405023104 listed 24 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K092992
- Listed FDA GUDID 00849405023104
- Registered EUDAMED B-00849405023104
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Bridge Foam Kit EUDAMEDBridge Dressing Kit GUDID
- Generic name
- Negative-pressure wound therapy system foam dressing, non-antimicrobial
- Device name
- XLR8 Bridge Foam Kit
- Model / reference
- XF-BKMF1 EUDAMEDXF-BDMF1 GUDID
- Primary DI / UDI-DI
- 00849405023104
- Basic UDI-DI
- B-00849405023104
- 510(k) Number
- FDA product code
- OMP
- EMDN code
- M04040601 Polyurethane dressings, non-combined
- GMDN term
- Negative-pressure wound therapy system foam dressing, non-antimicrobial
- Device class
- Class IIb EUDAMEDClass II GUDID
- Regulation number
- 878.4780
- System or procedure pack
- Procedure pack which is a device in itself
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Türkiye
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | XF-BKMF1 | XF-BDMF1 |
| Device class | Class IIb | Class II |
| Supplied sterile | Yes | No |
Registry differences
EUDAMED and FDA GUDID describe the same product (same UDI-DI) and state different values:
- Supplied sterile UDI-DI 00849405023104: EUDAMED states Yes, FDA GUDID states No.
Device class is stated on each registry's own scale: Class IIb 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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