Integra DP Valve System 902045

by Integra Neurosciences Implant (France)

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number10381780033400 UDI-DI	Date1 Oct 2015Listed	StatusListed GUDID: not in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Integra DP Valve System
Generic Name: Ventriculo-peritoneal/atrial shunt
Model / Ref / Catalog: 902045

Primary DI / UDI-DI: 10381780033400
510(k) Number: K152897
K861377
FDA Product Code: JXG
GMDN Term: Ventriculo-peritoneal/atrial shunt

Device Class: Class II
Regulation Number: 882.5550
GUDID distribution status: Not in Commercial Distribution

MRI Safety: MR Conditional

Properties

Sterile
Single Use
Implantable
Prescription Use
Convenience Kit
Lot / Batch Number
Expiration Date
Manufacturing Date

Other properties (6)

Contains Latex: No
Over-the-Counter: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Serial Number: No