DirectVision MA100143

by Percuvision, LLC

DirectVision MA100143 is an indwelling urethral catheterization kit made by Percuvision, LLC, listed in FDA GUDID since 23 Sep 2016 (UDI-DI 00855308006045), 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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00855308006045 UDI-DI	Date23 Sep 2016Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00855308006045

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: DirectVision
Generic name: Indwelling urethral catheterization kit, adult
Model / reference: MA100143

Primary DI / UDI-DI: 00855308006045
GMDN term: Indwelling urethral catheterization kit, adult

GUDID distribution status: In Commercial Distribution

Other devices from Percuvision, LLC

See all devices from Percuvision, LLC →

Properties

Supplied sterile
Single use
Prescription use
Convenience kit
Lot / batch number
Expiration date
Manufacturing date

Other properties (8, all answered No)