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Codman Microsensor® 626653US

by Integra LifeSciences Production Corporation

Codman Microsensor® 626653US is a Class II device made by Integra LifeSciences Production Corporation, listed in FDA GUDID since 1 Apr 2020 (UDI-DI 10381780514558), 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 Number10381780514558 UDI-DI Date1 Apr 2020ListedStatusListed 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  • Withdrawn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
Codman Microsensor®
Generic name
Intracranial pressure monitor
Model / Ref / Catalog
626653US
Primary DI / UDI-DI
10381780514558
FDA product code
GWM
GMDN term
Intracranial pressure monitor
Device class
Class II
Regulation number
882.1620
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

Related devices

Category: Intracranial pressure monitor

Other devices from Integra LifeSciences Production Corporation

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)