Device Explorer · FDA GUDID · GMDN 62494

Caecostomy tube

A sterile, thin, soft, hollow tube intended to be percutaneously placed and maintained in the caecum, following caecostomy, to permit instillation of fluids for colonic irrigation and evacuation of lower bowel contents through the anus, as an aid in the manage

US‑registered devices265in commercial distribution
Companies2labelers on GUDID
Single‑use100%of device records
Sterile97%labelled sterile
Prescription100%Rx‑only share
ImplantableYesGMDN flag
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Share of device records

Applied Medical Technology, Inc.26098%
Cook Incorporated52%

Top labelers

CompanyDevicesShare
Applied Medical Technology, Inc.26098%
Cook Incorporated52%

Company = labeler of record on GUDID. 2 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

MiniACEMiniACE Low Profile Antegrade Continence Enema IMiniACE®MiniACE™MiniACE™ Low Profile Antegrade Continence Enema MiniACE™ Low Profile Antegrade Continence Enema Chait

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

FDA product codes

CodeNameDevices
KNTTubes, Gastrointestinal (And Accessories)260
EXDIrrigator, Ostomy260
PIFGastrointestinal Tubes With Enteral Specific Connectors260
KNTTUBES, GASTROINTESTINAL (AND ACCESSORIES)4
GCDCONNECTOR, CATHETER1

GMDN & GCC registration

  • GMDN code 62494 · implantable
  • Single‑use 100% · sterile 97% · Rx‑only 100% · OTC 0%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Length (Centimeter) · 252Catheter Gauge (French) · 252Length (Inch) · 8

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

How many caecostomy tube products are registered in the US?

265 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Caecostomy tube", from 2 companies. The largest labeler is Applied Medical Technology, Inc. with 98% of records.

Which FDA product codes apply?

KNT (Tubes, Gastrointestinal (And Accessories)), EXD (Irrigator, Ostomy), PIF (Gastrointestinal Tubes With Enteral Specific Connectors), KNT (TUBES, GASTROINTESTINAL (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.

How do I get quotes?

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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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