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Compactcath 40788

by Compactcath, Inc 3 variants

Compactcath 40788 (1612) is a Class II device made by Compactcath, Inc, listed in FDA GUDID since 9 Dec 2016 (UDI-DI 00852141007024), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00852141007024 UDI-DI Date9 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  • Withdrawn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
Compactcath
Generic name
Single-administration urethral catheterization kit, single-use
Model / Ref / Catalog
40788, 1612
Primary DI / UDI-DI
00852141007024
FDA product code
EZD
GMDN term
Single-administration urethral catheterization kit, single-use
Device class
Class II
Regulation number
876.5130
GUDID distribution status
In Commercial Distribution
Size
Length — 16 Inch
Catheter Gauge — 12 French

Related devices

Category: Single-administration urethral catheterization kit, single-use

Similar devices

Other devices filed under FDA product code EZD (Catheter, Straight).

Other devices from Compactcath, Inc

See all devices from Compactcath, Inc →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
Other properties (11, all answered No)