Identity
- Trade Name
- EpiAccess Needle FDA UDI
- Generic Name
- Pericardiocentesis needle, single-use FDA UDI
- Model / Reference
- 0399-13950 FDA UDI
Identifiers
- Primary DI / UDI-DI
- B3000399139500 FDA UDI
- 510(k) Number
- K142245 FDA UDI
- FDA Product Code
- DYB FDA UDI
- GMDN Term
- Pericardiocentesis needle, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1340 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Pericardiocentesis needle, single-use
EpiAccess Needle by Epiep, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Pericardiocentesis needle, single-use.
- DLP® — MEDTRONIC, INC. · Class II
- PeriVac™ Kit — Boston Scientific · Class II
- PeriVac™ Kit — Boston Scientific · Class II
- PeriVac™ Kit — Boston Scientific · Class II
Cleared under the same submission
K142245 also covers:
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Epiep, Inc.
Sources (1)
- FDA UDI cff284a2-7ce5-471c-90f1-ea0b8dd545ae 33 fields · synced Jun 1, 2026