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Device Explorer · FDA GUDID · GMDN 35134

Dermatome blade, single-use

A surgical cutting device that is designed to be mounted onto a dermatome handle/handpiece (not included) and used to provide the cutting edge for the harvesting of skin grafts or excision of small skin lesions. It is available in various sizes. This is a sing

US‑registered devices77in commercial distribution
Companies17labelers on GUDID
Single‑use99%of device records
Sterile61%labelled sterile
Prescription32%Rx‑only share
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Share of device records

Jiangsu Mjd Medical Technology Co.,Ltd.2836%
Humeca B.V.912%
Swann-Morton Limited810%
Nouvag Ag68%
Integra Lifesciences Corporation45%
Aesculap Ag34%
Bioseal34%
Stryker Corporation23%

Top labelers

CompanyDevicesShare
Jiangsu Mjd Medical Technology Co.,Ltd.2836%
Humeca B.V.912%
Swann-Morton Limited810%
Nouvag Ag68%
Integra Lifesciences Corporation45%
Aesculap Ag34%
Bioseal34%
Stryker Corporation23%
De Soutter Medical Limited23%
Zimmer Orthopaedic Surgical Products, Inc.23%
Exsurco Medical, Inc.23%
Robbins Instruments Inc.23%

Company = labeler of record on GUDID. 17 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

NAMTDe Soutter MedicalSwann Morton Ltd.FEATHER SKIN GRAFT KNIFE BLADEMedicon TrayAESCULAPN/ADermatomeTissueMillXpansion® Micro-Autografting Kit2-inch ASD Excision ring blade4-inch ASD Excision ring bladeBioseal Inc.Padgett Replacement Dermatome Blades Non-SterilePadgett Replacement Dermatome Blades Sterile

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

FDA product codes

CodeNameDevices
GFDDermatome51
FZWExpander, Surgical, Skin Graft10
GFDDERMATOME5
GESBlade, Scalpel4
KDCINSTRUMENT, SURGICAL, DISPOSABLE3
GFEBRUSH, DERMABRASION, POWERED2

GMDN & GCC registration

  • GMDN code 35134 · non‑implantable
  • Single‑use 99% · sterile 61% · Rx‑only 32% · 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 (Millimeter) · 2Outer Diameter (Inch) · 2

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

How many dermatome blade, single-use products are registered in the US?

77 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Dermatome blade, single-use", from 17 companies. The largest labeler is Jiangsu Mjd Medical Technology Co.,Ltd. with 36% of records.

Which FDA product codes apply?

GFD (Dermatome), FZW (Expander, Surgical, Skin Graft), GFD (DERMATOME), GES (Blade, Scalpel)

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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