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Tough Cut Scissors 18.5cm (Non Sterile)
EUDAMEDFDA UDIClass I (EU MDR)
Ref 7913
Identity
- Trade Name
- Tough Cut Scissors 18.5cm (Non Sterile) EUDAMEDInstrapac FDA UDI
- Generic Name
- Cast cutting scissors FDA UDI
- Device Name
- Tough Cut Scissors EUDAMEDInstrapac Tough Cut Scissors Non-Sterile 18.5cm x 10 FDA UDI
- Model / Reference
- 7913 EUDAMEDFDA UDI
- Description
- Instrapac Tough Cut Scissors Non-Sterile 18.5cm x 10 FDA UDI
Identifiers
- Catalog Number
- 7913 FDA UDI
- Primary DI / UDI-DI
- 05010058079137 EUDAMEDFDA UDI
- Basic UDI-DI
- 5010058C01nT016G00B27 EUDAMED
- FDA Product Code
- LRW FDA UDI
- EMDN Code
- V0199 CUTTING DEVICES, SINGLE-USE - OTHER EUDAMED
- GMDN Term
- Cast cutting scissors FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Market of Registration
- Ireland 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
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
Dimensions & Sizes
- Size
- Length — 18.5 Centimeter FDA UDI
Category: Cranial bur, single-use
Tough Cut Scissors 18.5cm (Non Sterile) by Robinson Healthcare Ltd — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Cranial bur, single-use.
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- Bone cutters — WILSON (Shanghai) Medical Device Co., Ltd. · Class IIa
- GT PODO 5 mm rund/round Schaft 2, 35 x 35 — LUKAS-ERZETT GmbH & Co.KG · Class I
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 | 5010058C01nT016G00B27 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Robinson Healthcare Ltd
- EUDAMED SRN
- GB-MF-000016546
- Authorised Representative
- Advena Limited MT-AR-000000234
Sources (2)
- EUDAMED 16365327-5b87-436e-abc9-8cca0ad10d44 61 fields · synced Jun 17, 2026
- FDA UDI 2c41313c-d8b4-4fd3-91a1-54feaaa73b2e 37 fields · synced May 30, 2026