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Model 7A

FDA UDI

Class III (US FDA UDI)

by Cardio Command

Identity

Trade Name
Model 7A FDA UDI
Generic Name
External pacemaker, transoesophageal pacing FDA UDI
Device Name
Interface cable between 7A Stimulator and Model 3 preamplifier. FDA UDI
Model / Reference
7A/Mod 3 Interface cable FDA UDI
Description
Interface cable between 7A Stimulator and Model 3 preamplifier. FDA UDI

Identifiers

Catalog Number
0406 FDA UDI
Primary DI / UDI-DI
00856233005110 FDA UDI
PMA Number
P860008 FDA UDI
FDA Product Code
LPA FDA UDI
GMDN Term
External pacemaker, transoesophageal pacing 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

Category: External pacemaker, transoesophageal pacing

Model 7A by Cardio Command — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as External pacemaker, transoesophageal pacing.

Cleared under the same submission

P860008 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardio Command

Sources (1)

  • FDA UDI bec2048b-1022-4a6c-a715-6fa576a76189 36 fields · synced May 31, 2026