Identity
- Trade Name
- EnSite Precision™ FDA UDI
- Generic Name
- Electromagnetic surgical navigation device tracking system FDA UDI
- Device Name
- Field Frame FDA UDI
- Model / Reference
- H702469 FDA UDI
- Description
- Field Frame FDA UDI
Identifiers
- Catalog Number
- H702469 FDA UDI
- Primary DI / UDI-DI
- 05415067024695 FDA UDI
- FDA Product Code
- DQK FDA UDI
- GMDN Term
- Electromagnetic surgical navigation device tracking system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1425 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Electromagnetic surgical navigation device tracking system
EnSite Precision™ by St. Jude Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K160210 also covers:
- Advisor™ FL Mapping Catheter, Sensor Enabled™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
K182644 also covers:
K183128 also covers:
- Advisor™ — ST. JUDE MEDICAL, INC.
- Advisor™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
K201181 also covers:
- Advisor™ — ST. JUDE MEDICAL, INC.
- Advisor™ FL Mapping Catheter, Sensor Enabled™ — ST. JUDE MEDICAL, INC.
- Advisor™ HD Grid Mapping Catheter — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
- EnSite Precision™ — ST. JUDE MEDICAL, INC.
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
- St. Jude Medical, Inc.
Sources (1)
- FDA UDI 2220f19c-1033-477c-a020-7ed5cb76c040 37 fields · synced May 30, 2026