Identity
- Trade Name
- Merlin™ FDA UDI
- Generic Name
- External pacemaker analyser FDA UDI
- Device Name
- Adapter Medtronic Patient Cable Model 2292 FDA UDI
- Model / Reference
- EX3180 FDA UDI
- Description
- Adapter Medtronic Patient Cable Model 2292 FDA UDI
Identifiers
- Catalog Number
- EX3180 FDA UDI
- Primary DI / UDI-DI
- 05414734503136 FDA UDI
- FDA Product Code
- NIK FDA UDI
- GMDN Term
- External pacemaker analyser FDA UDI
Classification
- Device Class
- Class III 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
Dimensions & Sizes
- Size
- Length — 10 Inch FDA UDI
Category: External pacemaker analyser
Merlin™ by St. Jude Medical, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as External pacemaker analyser.
- External Pacemaker Analyzer — Netech Corp. · Class II
- External Pacemaker Ananlyzer — Netech Corp. · Class II
- External Pacemaker Analyzer — Netech Corp. · Class II
- Merlin™ — ST. JUDE MEDICAL, INC. · Class III
- Merlin™ — ST. JUDE MEDICAL, INC. · Class III
- Merlin™ — ST. JUDE MEDICAL, INC. · Class III
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 III | Pending data |
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Manufacturer
- Manufacturer
- St. Jude Medical, Inc.
Sources (1)
- FDA UDI 155aefa7-7550-4e1c-b416-5edb5f418417 37 fields · synced May 30, 2026