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Swann-Morton

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref PC25 - Smiths No. 15 Non Sterile Disposable ScalpelsModel 23 / 40 / 35 / LC / NU / PC Codes

by Swann-Morton Ltd

Identity

Trade Name
Swann-Morton EUDAMED
Swann Morton Ltd. FDA UDI
Generic Name
Scalpel, single-use FDA UDI
Device Name
Swann-Morton Non-Sterile Disposable Scalpel EUDAMED
A sterile, hand held, manual surgical instrument constructed as a one piece handle and scalpel blade (not an exchangeable component) used by the operator to manually cut or dissect tissue. The blade is typically made of high grade stainless steel alloy or carbon steel and the handle is often made of plastic. This is a single use device. FDA UDI
Model / Reference
23 / 40 / 35 / LC / NU / PC Codes EUDAMED
PC25 - Smiths No. 15 Non Sterile Disposable Scalpels EUDAMED
SMITHS No. 15 NON STERILE DISPOSABLE SCALPELS FDA UDI
Description
A sterile, hand held, manual surgical instrument constructed as a one piece handle and scalpel blade (not an exchangeable component) used by the operator to manually cut or dissect tissue. The blade is typically made of high grade stainless steel alloy or carbon steel and the handle is often made of plastic. This is a single use device. FDA UDI

Identifiers

Catalog Number
PC25 FDA UDI
Primary DI / UDI-DI
05033955140250 EUDAMEDFDA UDI
Basic UDI-DI
50339550NONSTDISPSH9 EUDAMED
Unit of Use DI
05063043140251 EUDAMED
FDA Product Code
GDX FDA UDI
EMDN Code
V010102 SCALPELS WITHOUT SAFETY SYSTEMS, SINGLE-USE EUDAMED
GMDN Term
Scalpel, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Market of Registration
France EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI

Category: Scalpel, single-use

Swann-Morton by Swann-Morton Ltd — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Scalpel, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Swann-Morton Ltd
EUDAMED SRN
GB-MF-000001890
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED bb88e940-766b-41f6-8302-b61d59ca7937 61 fields · synced May 30, 2026
  • FDA UDI 73f5ea98-f823-4521-ad13-e6dbaf317935 35 fields · synced May 30, 2026