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Osv II® 9OS712

by Integra LifeSciences Switzerland Sàrl

Osv II® 9OS712 is a Class II device made by Integra LifeSciences Switzerland Sàrl, listed in FDA GUDID since 1 Oct 2015 (UDI-DI 10381780036074), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10381780036074 UDI-DI Date1 Oct 2015ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Osv II®
Generic name
Ventriculo-peritoneal/atrial shunt
Model / Ref / Catalog
9OS712
Primary DI / UDI-DI
10381780036074
FDA product code
JXG
GMDN term
Ventriculo-peritoneal/atrial shunt
Device class
Class II
Regulation number
882.5550
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

Related devices

Category: Ventriculo-peritoneal/atrial shunt

Other devices from Integra LifeSciences Switzerland Sàrl

See all devices from Integra LifeSciences Switzerland Sàrl →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (7, all answered No)