Identity
- Trade Name
- Premicath FDA UDI
- Generic Name
- Peripherally-inserted central venous catheter FDA UDI
- Device Name
- PREMICATH 28 G (1 FR) 20 CM CATHETER AND SPLITTING NEEDLE FDA UDI
- Model / Reference
- 1261.20G FDA UDI
- Description
- PREMICATH 28 G (1 FR) 20 CM CATHETER AND SPLITTING NEEDLE FDA UDI
Identifiers
- Catalog Number
- 1261.20G FDA UDI
- Primary DI / UDI-DI
- 08498840008515 FDA UDI
- 510(k) Number
- K954302 FDA UDI
- FDA Product Code
- LJS FDA UDI
- GMDN Term
- Peripherally-inserted central venous catheter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5970 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 24 Millimeter FDA UDI
Category: Peripherally-inserted central venous catheter
Premicath by Vygon Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Peripherally-inserted central venous catheter.
- BioFlo — NAVILYST MEDICAL, INC. · Class II
- Synergy — Health Line International Corp · Class II
- ARROW — TELEFLEX INCORPORATED · Class II
- ARROW — TELEFLEX INCORPORATED · Class II
- PowerPICC — Bard Access Systems, Inc. · Class II
- ARROW — TELEFLEX INCORPORATED · Class II
- PowerPICC Provena — Bard Access Systems, Inc. · Class II
- BioFlo — NAVILYST MEDICAL, INC. · Class II
Cleared under the same submission
K954302 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
- Vygon Corp.
Sources (1)
- FDA UDI 34871b96-3406-4375-b9a2-9ba00b9e5ebf 37 fields · synced May 30, 2026