Identity
- Trade Name
- ARROW FDA UDI
- Generic Name
- Epidural anaesthesia set, non-medicated FDA UDI
- Device Name
- ARROW® Epidural Catheterization Set with FlexTip Plus(R), Closed Tip Multi-Port Catheter FDA UDI
- Model / Reference
- IPN040178 FDA UDI
- Description
- ARROW® Epidural Catheterization Set with FlexTip Plus(R), Closed Tip Multi-Port Catheter FDA UDI
Identifiers
- Catalog Number
- MP-17019-TIG FDA UDI
- Primary DI / UDI-DI
- 00801902070173 FDA UDI
- FDA Product Code
- CAZ FDA UDI
- GMDN Term
- Epidural anaesthesia set, non-medicated FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5140 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
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
No
FDA UDI
MR Conditional FDA UDI
Dimensions & Sizes
- Size
- Length — 90 Centimeter FDA UDI
Category: Epidural anaesthesia set, non-medicated
Arrow by Teleflex Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Teleflex Incorporated
Sources (1)
- FDA UDI 83e232a7-b587-4c03-91d0-14ad236c5fb7 36 fields · synced Jun 8, 2026