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Integra® NL8501381

by Integra Lifesciences Corp.

Integra® NL8501381 is a Class II device made by Integra Lifesciences Corp., listed in FDA GUDID since 15 Dec 2016 (UDI-DI 10381780072324), 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 Number10381780072324 UDI-DI Date15 Dec 2016ListedStatusListed 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  • Withdrawn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
Integra®
Generic name
Peritoneal/atrial cerebrospinal fluid catheter
Model / Ref / Catalog
NL8501381
Primary DI / UDI-DI
10381780072324
FDA product code
JXG
GMDN term
Peritoneal/atrial cerebrospinal fluid catheter
Device class
Class II
Regulation number
882.5550
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

Related devices

Category: Peritoneal/atrial cerebrospinal fluid catheter

Similar devices in this category

Other devices filed under Peritoneal/atrial cerebrospinal fluid catheter.

Other devices from Integra Lifesciences Corp.

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Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)