← Back to catalogue
EMI Micro Vessel Dilators
EUDAMEDFDA UDIClass I (EU MDR)
Ref EMI093KT-L14-HG-KT-0.1Model Vessel Dilators
Identity
- Trade Name
- EMI Micro Vessel Dilators EUDAMEDEMI Super Micro Vessel Dilators FDA UDI
- Generic Name
- Surgical soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
- Device Name
- EMI Micro Vessel Dilators EUDAMEDUse for pinching or grasping skin, tissue, foreign substance etc. during medical treatment or surgery. FDA UDI
- Model / Reference
- Vessel Dilators EUDAMEDEMI093KT-L14-HG-KT-0.1 EUDAMEDEMI093KT FDA UDI
- Description
- Use for pinching or grasping skin, tissue, foreign substance etc. during medical treatment or surgery. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04582486866791 EUDAMEDFDA UDI
- Basic UDI-DI
- 458248686SMVDQ6 EUDAMED
- Direct Marketing DI
- 04582486866791 EUDAMED
- FDA Product Code
- HTD FDA UDI
- EMDN Code
- L1003 MICROSURGERY FORCEPS, REUSABLE EUDAMED
- GMDN Term
- Surgical soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Market of Registration
- Italy EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
Yes
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
EMI Micro Vessel Dilators by Emi Factory Co., 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 | 458248686SMVDQ6 | 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
- Emi Factory Co., Ltd.
- EUDAMED SRN
- JP-MF-000025742
- Authorised Representative
- Mitaka Europe GmbH DE-AR-000006361
Sources (2)
- EUDAMED 76fb7a3b-3fb4-4f04-a840-a707ea7c7e31 61 fields · synced May 30, 2026
- FDA UDI 2e730746-c0d0-4f36-b4ea-78a9ba077213 34 fields · synced May 30, 2026