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UDI Compass
Unknown / Not in EUDAMED

Snapshot 2026-10-09 · Link to EUDAMED

Percuflex™

UDI-DI 08714729067641Basic UDI-DI 01915060000000000000411MR

Class IIb · MDR · Boston Scientific Corporation

Identification
Model
—
Issuing agency
GS1
Device status
active
Sterile
Yes
Implantable
Yes
Measuring function
No
Reusable surgical
No
Certificates

3827895TD05

EU technical documentation assessment · unknown

Notified body: DEKRA Certification B.V. (0344)

Valid from 2024-10-15 · Expiry 2028-12-07

Scope not stated in certificate data.

Certificate’s own scope text — not a compliance opinion from UDI Compass.

Manufacturer

Boston Scientific Corporation

SRN US-MF-000004702

US · Marlborough

manufacturer

Authorised representative: Boston Scientific Limited (IE-AR-000003840)

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Showing 12 of 46 other UDI-DIs.

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Canonical device page: /device/percuflextm-7641 · UDI page: /udi/08714729067641

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