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Merlin.net

FDA UDI

Class III (US FDA UDI)

by St. Jude Medical, Inc.

Identity

Trade Name
Merlin.net FDA UDI
Generic Name
Transtelephonic implantable pacemaker analysis system FDA UDI
Device Name
Patient Interactive Website FDA UDI
Model / Reference
MN5000 FDA UDI
Description
Patient Interactive Website FDA UDI

Identifiers

Catalog Number
MN5000 FDA UDI
Primary DI / UDI-DI
05414734509732 FDA UDI
FDA Product Code
NIK FDA UDI
OSR FDA UDI
NKE FDA UDI
LWP FDA UDI
PNJ FDA UDI
LWS FDA UDI
LWO FDA UDI
DXY FDA UDI
NVZ FDA UDI
GMDN Term
Transtelephonic implantable pacemaker analysis system FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
870.3610 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: Transtelephonic implantable pacemaker analysis system

Merlin.net by St. Jude Medical, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Transtelephonic implantable pacemaker analysis system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
St. Jude Medical, Inc.

Sources (1)

  • FDA UDI 54a47eb9-bfeb-4735-816b-d0fb3e21d153 35 fields · synced Jun 8, 2026