Identity
- Trade Name
- 3F PRO-PICC®CT FDA UDI
- Generic Name
- Peripherally-inserted central venous catheter FDA UDI
- Device Name
- 5F X 55CM DUAL LUMEN5F X 55CM DU PRO-PICC®CT CATHETHER ONL FDA UDI
- Model / Reference
- MD17035200 FDA UDI
- Description
- 5F X 55CM DUAL LUMEN5F X 55CM DU PRO-PICC®CT CATHETHER ONL FDA UDI
Identifiers
- Catalog Number
- MD17035200 FDA UDI
- Primary DI / UDI-DI
- 00884908139396 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
- Not 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
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
No
FDA UDI
3f Pro-Picc®ct by Medical Components Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Medical Components Inc
Sources (1)
- FDA UDI fe4191b0-67a7-45b2-9a8c-f5527690958c 36 fields · synced Jun 1, 2026