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Epimed International, Inc.
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref 134-1430Model Flexible Epidural Introducer (FIC)/Blunt Cannula Access (BAC)
Identity
- Trade Name
- Epimed International,Inc. EUDAMEDEpimed FDA UDI
- Generic Name
- Non-vascular catheter introduction set FDA UDI
- Device Name
- Percutaneous Introducer w/ 14g RW x 2.1" B Bevel FDA UDI
- Model / Reference
- Flexible Epidural Introducer (FIC)/Blunt Cannula Access (BAC) EUDAMED134-1430 EUDAMEDFDA UDI
- Description
- Percutaneous Introducer w/ 14g RW x 2.1" B Bevel FDA UDI
Identifiers
- Catalog Number
- 134-1430 FDA UDI
- Primary DI / UDI-DI
- 00818788020901 EUDAMEDFDA UDI
- Basic UDI-DI
- 081878802FEIKH EUDAMED
- 510(k) Number
- K051860 FDA UDI
- FDA Product Code
- MIA FDA UDI
- EMDN Code
- A019013 PERCUTANEOUS NEEDLES EUDAMED
- GMDN Term
- Non-vascular catheter introduction set FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 868.5150 FDA UDI
- Market of Registration
- Netherlands EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
Yes
EUDAMED
Measuring Function
Yes
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Ethylene Oxide FDA UDI
MR Unsafe FDA UDI
Dimensions & Sizes
- Size
- Needle Gauge — 14 Gauge FDA UDILength — 3 Inch FDA UDI
Epimed International, Inc. by Epimed International, Inc. — Class IIa — 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 | 081878802FEIKH | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Epimed International, Inc.
- EUDAMED SRN
- US-MF-000010774
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (2)
- EUDAMED d42205f7-3d66-4621-8149-555f26b8b0f3 61 fields · synced Jun 6, 2026
- FDA UDI 9a02e59c-5f80-4597-ac39-0cf776676d54 38 fields · synced May 27, 2026