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Device Explorer · FDA GUDID · GMDN 64696

Non-ISO80369-standardized small-bore multichannel connector, single-use

A small, non-powered, noninvasive, small-bore tubular connector with three or more connections (typically barbed, bayonet, conical, threaded and/or non-Luer-slip), none of which are designed according to ISO 80369 (standard for small-bore connectors for liquid

US‑registered devices134in commercial distribution
Companies3labelers on GUDID
Single‑use100%of device records
Sterile66%labelled sterile
Prescription94%Rx‑only share
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Share of device records

Novosci Corp.10981%
Cardinal Health 200, Llc2418%
Cardinal Health, Inc.11%

Top labelers

CompanyDevicesShare
Novosci Corp.10981%
Cardinal Health 200, Llc2418%
Cardinal Health, Inc.11%

Company = labeler of record on GUDID. 3 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

CARDINAL HEALTH"CONNECTOR, Y 1/2"" X 1/2"" X 1/4""""CONNECTOR, Y 1/2"" X 1/2"" X 3/8""""CONNECTOR, Y 1/4"" X 3/8"" X 3/8""""CONNECTOR, Y 3/8"" X 1/4"" X 3/8"" W/LUER""CONNECTOR, Y 3/8"" X 1/4"" X 3/8""""CONNECTOR, Y 1/2"" X 3/8"" X 3/8"" W/LUER""CONNECTOR, Y 1/2"" X 3/8"" X 3/8""""CONNECTOR, Y 3/8"" X 1/4"" X 1/4"" W/LUER""CONNECTOR, Y 3/8"" X 1/4"" X 1/4""""CONNECTOR, Y 1/4"" X 3/16"" X 3/16""""CONNECTOR, EQUAL Y 1/2"" W/LUER""CONNECTOR, EQUAL Y 3/8""""CONNECTOR, EQUAL Y 1/2"" ""CONNECTOR, EQUAL Y 3/8"" W/LUER""CONNECTOR, EQUAL Y 3/8"" "

Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.

FDA product codes

CodeNameDevices
KRIAccessory Equipment, Cardiopulmonary Bypass57
KOCAccessories, Blood Circuit, Hemodialysis34
DTLAdaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass20
BYXTUBING, PRESSURE AND ACCESSORIES14
GCDCONNECTOR, CATHETER13
BYYTUBE, ASPIRATING, FLEXIBLE, CONNECTING5

GMDN & GCC registration

  • GMDN code 64696 · non‑implantable
  • Single‑use 100% · sterile 66% · Rx‑only 94% · OTC 4%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Catheter Gauge (French) · 3Outer Diameter (Millimeter) · 2Lumen/Inner Diameter (Millimeter) · 2Width (Millimeter) · 2Length (Millimeter) · 1Height (Millimeter) · 1

Use these as the dimensions to specify in a tender line.

How many non-iso80369-standardized small-bore multichannel connector, single-use products are registered in the US?

134 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Non-ISO80369-standardized small-bore multichannel connector, single-use", from 3 companies. The largest labeler is Novosci Corp. with 81% of records.

Which FDA product codes apply?

KRI (Accessory Equipment, Cardiopulmonary Bypass), KOC (Accessories, Blood Circuit, Hemodialysis), DTL (Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass), BYX (TUBING, PRESSURE AND ACCESSORIES)

Is this the same as UAE/GCC registration?

No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.

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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.

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