Identity
- Trade Name
- FLEXITIP FDA UDI
- Generic Name
- Electrical-only medical device connection cable, reusable FDA UDI
- Device Name
- CONMED FLEXITIP DISPOSABLE SCLEROTHERAPY NEEDLE, 5 MM X 160 CM FDA UDI
- Model / Reference
- 000199 FDA UDI
- Description
- CONMED FLEXITIP DISPOSABLE SCLEROTHERAPY NEEDLE, 5 MM X 160 CM FDA UDI
Identifiers
- Catalog Number
- 000199 FDA UDI
- Primary DI / UDI-DI
- 30653405051200 FDA UDI
- FDA Product Code
- GAA FDA UDI
- GMDN Term
- Electrical-only medical device connection cable, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 2.3 Millimeter FDA UDIWeight — 25 Gram FDA UDILength — 5 Millimeter FDA UDILength — 160 Centimeter FDA UDI
Category: Electrical-only medical device connection cable, reusable
Flexitip by Conmed Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Electrical-only medical device connection cable, reusable.
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- ECG Cable — Edan Instruments,Inc. · Class I
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 I | Pending data |
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Manufacturer
- Manufacturer
- Conmed Corporation
Sources (1)
- FDA UDI 74ba2e52-45da-444c-aeb6-61bef5650af0 36 fields · synced May 30, 2026