Identity
- Trade Name
- MEDCOMP TESIO CATHETERSMEDCOMP TESIO CATHETERS FDA UDI
- Generic Name
- Double-lumen haemodialysis catheter, implantable FDA UDI
- Device Name
- 10F BIO-FLEX®TESIO® CATHETERS W/STYLETCATHETERS W/ST (ARTERIAL CUFF-27CM FROM(ARTERIA TIP) (VENOUS CUFF-30CM FROMTIP) TIP)TIP) FDA UDI
- Model / Reference
- DBFL-6S FDA UDI
- Description
- 10F BIO-FLEX®TESIO® CATHETERS W/STYLETCATHETERS W/ST (ARTERIAL CUFF-27CM FROM(ARTERIA TIP) (VENOUS CUFF-30CM FROMTIP) TIP)TIP) FDA UDI
Identifiers
- Catalog Number
- DBFL-6S FDA UDI
- Primary DI / UDI-DI
- 00884908141160 FDA UDI
- FDA Product Code
- MSD FDA UDI
- GMDN Term
- Double-lumen haemodialysis catheter, implantable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.5540 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
MR Conditional FDA UDI
Medcomp Tesio Cathetersmedcomp Tesio Catheters 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 8bdc7371-97cc-4eaf-a3ab-afe3e64c64dd 36 fields · synced Jun 1, 2026