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Swann-Morton

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 1922 - Bulk No. 10A Stainless Blades Model 01 / 19 / 30 / R Codes

by Swann-Morton Ltd

Identity

Trade Name
Swann-Morton EUDAMED
Swann Morton Ltd. FDA UDI
Generic Name
Manual scalpel blade, single-use FDA UDI
Device Name
Swann-Morton Non Sterile Standard Surgical Blades EUDAMED
Blade,scalpel, single use. A component of a surgical instrument (scalpel) that is designed to be attached to the scalpel handle. It is capable of cutting through tissue when moved with downward pressure. This device is disposable. FDA UDI
Model / Reference
01 / 19 / 30 / R Codes EUDAMED
1922 - Bulk No. 10A Stainless Blades EUDAMED
BULK No.10A STAINLESS BLADES FDA UDI
Description
Blade,scalpel, single use. A component of a surgical instrument (scalpel) that is designed to be attached to the scalpel handle. It is capable of cutting through tissue when moved with downward pressure. This device is disposable. FDA UDI

Identifiers

Catalog Number
1922 FDA UDI
Primary DI / UDI-DI
05033955019228 EUDAMEDFDA UDI
Basic UDI-DI
50339550NONSTBLADES6V EUDAMED
Unit of Use DI
05063043019229 EUDAMED
FDA Product Code
GES FDA UDI
EMDN Code
V010302 BLADES WITHOUT SAFETY SYSTEMS, SINGLE-USE - NOT INCLUDED IN OTHER CLASSES EUDAMED
GMDN Term
Manual scalpel blade, 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: Manual scalpel blade, 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 Manual scalpel blade, 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 b853e97c-600e-4ff9-b8ea-fb3bd95788fe 61 fields · synced May 30, 2026
  • FDA UDI 83c55bce-df9e-40b3-8e42-88d33d94b511 35 fields · synced May 30, 2026