Identity
- Trade Name
- Emprint SX FDA UDI
- Generic Name
- Microwave ablation system probe, non-powered FDA UDI
- Device Name
- Long Navigation Antenna with Thermosphere Technology FDA UDI
- Model / Reference
- CA30L2N FDA UDI
- Description
- Long Navigation Antenna with Thermosphere Technology FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10884521703292 FDA UDI
- FDA Product Code
- NEY FDA UDIGEI FDA UDI
- GMDN Term
- Microwave ablation system probe, non-powered FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4400 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
Yes
FDA UDI
MR Unsafe FDA UDI
Dimensions & Sizes
- Size
- Length — 30 Centimeter FDA UDI
Category: Microwave ablation system probe, non-powered
Emprint SX by Covidien LP — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Microwave ablation system probe, non-powered.
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- Swift® — Emblation , Ltd. · Class I
- Microwave Ablation Antennas — Canyon Medical Inc. · Class IIb
- Microwave Ablation Antennas — Canyon Medical Inc. · Class IIb
- Microwave Ablation Antennas — Canyon Medical Inc. · Class IIb
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
- Covidien LP
Sources (1)
- FDA UDI 3896cd4d-5d55-4016-84d1-0a68e6468c6b 36 fields · synced May 31, 2026