Identity
- Trade Name
- EnSite Precision™ FDA UDI
- Generic Name
- Medical table clamp FDA UDI
- Device Name
- Field Frame Bracket FDA UDI
- Model / Reference
- H702472 FDA UDI
- Description
- Field Frame Bracket FDA UDI
Identifiers
- Catalog Number
- H702472 FDA UDI
- Primary DI / UDI-DI
- 05415067024725 FDA UDI
- FDA Product Code
- DQK FDA UDI
- GMDN Term
- Medical table clamp 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Medical table clamp
EnSite Precision™ by St. Jude Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Medical table clamp.
- Dual Pendant Holder — Mizuho Orthopedic Systems, Inc. · Class I
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- SPRINGLOC CLAMP JPN — Skytron, LLC · Class I
- De Mayo Push Button™ Clamp — INNOVATIVE MEDICAL PRODUCTS, INC. · Class I
- Radial clamp — Reison Medical AB · Class I
- Secure-Release — STERIS CORPORATION · Class I
- COUPLER II RADIOLUCENT DORO ADAPTER, REFURBISHED — Mizuho Orthopedic Systems, Inc. · Class I
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.
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 |
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Manufacturer
- Manufacturer
- St. Jude Medical, Inc.
Sources (1)
- FDA UDI aee6e67f-190d-4b85-83c8-f98f3e92ca78 37 fields · synced May 30, 2026