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Device Explorer · FDA GUDID · GMDN 13702

Neurosurgical sponge

A sterile absorbent material intended to be used on the brain to remove blood and other fluids during an operation. This is a single-use device.

US‑registered devices257in commercial distribution
Companies10labelers on GUDID
Single‑use100%of device records
Sterile92%labelled sterile
Prescription58%Rx‑only share
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Share of device records

American Surgical Company, Llc9838%
Deroyal Industries, Inc.5220%
Integra Lifesciences Production Corporation4116%
First Aid Bandage Co Inc229%
Medline Industries, Inc.197%
Teleflex Incorporated145%
Amd Medicom Inc73%
Bioseal21%

Top labelers

CompanyDevicesShare
American Surgical Company, Llc9838%
Deroyal Industries, Inc.5220%
Integra Lifesciences Production Corporation4116%
First Aid Bandage Co Inc229%
Medline Industries, Inc.197%
Teleflex Incorporated145%
Amd Medicom Inc73%
Bioseal21%
Suzhou Texnet Co., Ltd.10%
Cardinal Health 200, Llc10%

Company = labeler of record on GUDID. 10 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Suzhou TexnetPILLINGAtlas Choice Cranial Pattie CollectionAtlas Choice Microsurgery Pattie CollectionTapered DelicotCustom Telfa PackDeRoyalBioseal Inc.ArgyleArmourSorbTelfaRay-CotFABCOUniqcotDelicotMEDLINE

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

FDA product codes

CodeNameDevices
HBANeurosurgical Paddie98
EFQGAUZE/SPONGE, INTERNAL78
HBANeurosurgical paddie61
GDYGAUZE/SPONGE, INTERNAL, X-RAY DETECTABLE54
HBANEUROSURGICAL PADDIE41
EFQGauze/Sponge, Internal29

GMDN & GCC registration

  • GMDN code 13702 · non‑implantable
  • Single‑use 100% · sterile 92% · Rx‑only 58% · 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

Width (Inch) · 35Length (Inch) · 35Width (Millimeter) · 22Length (Millimeter) · 22Length (Meter) · 2Outer Diameter (Millimeter) · 2

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

How many neurosurgical sponge products are registered in the US?

257 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Neurosurgical sponge", from 10 companies. The largest labeler is American Surgical Company, Llc with 38% of records.

Which FDA product codes apply?

HBA (Neurosurgical Paddie), EFQ (GAUZE/SPONGE, INTERNAL), HBA (Neurosurgical paddie), GDY (GAUZE/SPONGE, INTERNAL, X-RAY DETECTABLE)

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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