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Q Tech

FDA UDI

Class III (US FDA UDI)

by Cameron Health, Inc.

Identity

Trade Name
Q TECH FDA UDI
Generic Name
Cardiac pulse generator programmer FDA UDI
Device Name
Programmer for the S-ICD® System FDA UDI
Model / Reference
3200 FDA UDI
Description
Programmer for the S-ICD® System FDA UDI

Identifiers

Primary DI / UDI-DI
00802526542206 FDA UDI
PMA Number
P110042 FDA UDI
FDA Product Code
LWS FDA UDI
GMDN Term
Cardiac pulse generator programmer FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Q Tech by Cameron Health, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

P110042 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cameron Health, Inc.

Sources (1)

  • FDA UDI 89c661c9-d82b-4825-b9dc-50dbc733faaa 35 fields · synced Jun 8, 2026