FlexTip Plus Epidural Catheterization Kit (UDI 10801902197679)
Manufactured by Arrow International LLC (Subsidiary of Teleflex Incorporated)
Device Regulatory Overview
The FlexTip Plus Epidural Catheterization Kit (Model/Catalog Number: DE-05501-KLD) is a medical device manufactured by Arrow International LLC (Subsidiary of Teleflex Incorporated). This product is indexed under FDA Product Code / Category Classification N02010199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DE-05501-KLD
- Product Code / EMDN
- N02010199
- Device Name
- Anesthesia Procedure Packs - Catheters
- Database Sync Date
- 2026-08-09 16:59:20
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of FlexTip Plus Epidural Catheterization Kit?
The registered manufacturer of record for FlexTip Plus Epidural Catheterization Kit is Arrow International LLC (Subsidiary of Teleflex Incorporated).
What is the Primary UDI-DI identifier for FlexTip Plus Epidural Catheterization Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10801902197679.
What classification code is assigned to this device?
This device is registered under product classification code N02010199.
Similar Classification Devices (N02010199)
Other Devices by Arrow International LLC (Subsidiary of Teleflex Incorporated)
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