← Back to catalogue
Swann-Morton Limited
EUDAMEDFDA UDIClass I (EU MDR)
Ref 4026 - Non-Sterile Retractable Scalpel Stitch CutterModel 19 / 35 /40 Codes
Identity
- Trade Name
- Swann-Morton Limited EUDAMEDSwann Morton Ltd. FDA UDI
- Generic Name
- Suture cutter, reusable FDA UDI
- Device Name
- Swann-Morton Non Sterile Stitch Cutters EUDAMEDSuture cutter, reusable. A dedicated hand-held surgical instrument designed for cutting sutures. It will typically have a protected scalpel-like blade which may be fixed or have a scissors-like cutting action. This is a reusable device. FDA UDI
- Model / Reference
- 19 / 35 /40 Codes EUDAMED4026 - Non-Sterile Retractable Scalpel Stitch Cutter EUDAMEDSTITCH CUTTER BULK NON STERILE RETRACTABLE SCALPELS FDA UDI
- Description
- Suture cutter, reusable. A dedicated hand-held surgical instrument designed for cutting sutures. It will typically have a protected scalpel-like blade which may be fixed or have a scissors-like cutting action. This is a reusable device. FDA UDI
Identifiers
- Catalog Number
- 4026 FDA UDI
- Primary DI / UDI-DI
- 05033955040260 EUDAMEDFDA UDI
- Basic UDI-DI
- 50339550NSTSCNE EUDAMED
- Unit of Use DI
- 05063043040261 EUDAMED
- FDA Product Code
- FZT FDA UDI
- EMDN Code
- V0102 STAPLE REMOVER KNIVES, SINGLE-USE EUDAMED
- GMDN Term
- Suture cutter, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA 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
Radiation Sterilization FDA UDI
Swann-Morton Limited by Swann-Morton Ltd — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 50339550NSTSCNE | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Swann-Morton Ltd
- EUDAMED SRN
- GB-MF-000001890
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (2)
- EUDAMED 562d08b9-f9e7-4267-b214-25202bf0666b 61 fields · synced Jul 29, 2026
- FDA UDI 4b56c88c-726f-4f45-83da-2c83f08873f0 35 fields · synced May 30, 2026