Device Explorer · FDA GUDID · GMDN 32572

Cottonoid pad

A cushion-like mass made of cotton or man-made fibres used during surgery (e.g., neurosurgery) to protect tissue, absorb fluids, and/or stop bleeding. This is a single-use device.

US‑registered devices234in commercial distribution
Companies4labelers on GUDID
Single‑use100%of device records
Sterile91%labelled sterile
Prescription0%Rx‑only share
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Share of device records

Omt, Llc16370%
American Surgical Company, Llc5423%
Cardinal Health, Inc.156%
Cardinal Health 200, Llc21%

Top labelers

CompanyDevicesShare
Omt, Llc16370%
American Surgical Company, Llc5423%
Cardinal Health, Inc.156%
Cardinal Health 200, Llc21%

Company = labeler of record on GUDID. 4 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

KendallAmericotDermaceaSure CareUltracotOMT LLCSpetzler Neuro PattiesSpetzler - OMTCuritySimplicity

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

FDA product codes

CodeNameDevices
HBANeurosurgical Paddie217
NABGauze / sponge,nonresorbable for external use10
KMEBEDDING, DISPOSABLE, MEDICAL6
EYQGARMENT, PROTECTIVE, FOR INCONTINENCE4

GMDN & GCC registration

  • GMDN code 32572 · non‑implantable
  • Single‑use 100% · sterile 91% · Rx‑only 0% · OTC 7%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Length (Inch) · 18Width (Inch) · 18

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

How many cottonoid pad products are registered in the US?

234 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Cottonoid pad", from 4 companies. The largest labeler is Omt, Llc with 70% of records.

Which FDA product codes apply?

HBA (Neurosurgical Paddie), NAB (Gauze / sponge,nonresorbable for external use), KME (BEDDING, DISPOSABLE, MEDICAL), EYQ (GARMENT, PROTECTIVE, FOR INCONTINENCE)

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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