6033112

by Gambro Dasco SpA

6033112 (107620) is a Class II device made by Gambro Dasco SpA, listed in FDA GUDID since 31 May 2017 (UDI-DI 07332414075439), 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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number07332414075439 UDI-DI	Date31 May 2017Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 07332414075439

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic name: Haemodialysis blood tubing set, single-use
Model / Ref / Catalog: 6033112, 107620

Primary DI / UDI-DI: 07332414075439
FDA product code: KOC
GMDN term: Haemodialysis blood tubing set, single-use

Device class: Class II
Regulation number: 876.5820
GUDID distribution status: In Commercial Distribution

Other devices from Gambro Dasco SpA

6038020

Class II
6033765

Class I
6032403

Class II
6431233B

Class II

See all devices from Gambro Dasco SpA →

Properties

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

Other properties (9, all answered No)