Identity
- Trade Name
- Retrax Cord Cutter EUDAMEDFDA UDI
- Generic Name
- General-purpose surgical scissors, reusable FDA UDI
- Device Name
- Generic Devices EUDAMEDStainless steel retraction cord cutter with micro serration. Autoclavable FDA UDI
- Model / Reference
- 26440 EUDAMEDFDA UDI
- Description
- Stainless steel retraction cord cutter with micro serration. Autoclavable FDA UDI
Identifiers
- Catalog Number
- 26440 FDA UDI
- Primary DI / UDI-DI
- 00310866000732 EUDAMEDFDA UDI
- Basic UDI-DI
- 03108669002HH EUDAMED
- FDA Product Code
- EIF FDA UDI
- EMDN Code
- L010499 SURGICAL SCISSORS, REUSABLE - OTHER EUDAMED
- GMDN Term
- General-purpose surgical scissors, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 872.4565 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Retrax Cord Cutter by Pascal Company, Inc. — 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 | 03108669002HH | 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
- Pascal Company Inc.
- EUDAMED SRN
- US-MF-000032036
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (2)
- EUDAMED b3ec1e74-12f2-43f0-93a3-2d4941fa4388 61 fields · synced Jul 8, 2026
- FDA UDI f8edf0b8-6e35-4f55-b15c-dc393d318d69 35 fields · synced May 30, 2026