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Guardian Programmer Model PROG-004

FDA UDI

Class III (US FDA UDI)

by Avertix Medical Inc.

Identity

Trade Name
Guardian Programmer Model PROG-004 FDA UDI
Generic Name
Implantable cardiac device management application software FDA UDI
Device Name
PROG-004 Kit (US) FDA UDI
Model / Reference
0217-2100-004#P18 FDA UDI
Description
PROG-004 Kit (US) FDA UDI

Identifiers

Catalog Number
0217-2100-004#P18 FDA UDI
Primary DI / UDI-DI
00850012625162 FDA UDI
PMA Number
P150009 FDA UDI
FDA Product Code
QBI FDA UDI
GMDN Term
Implantable cardiac device management application software 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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Category: Implantable cardiac device management application software

Guardian Programmer Model PROG-004 by Avertix Medical Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Implantable cardiac device management application software.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6f28c94e-0289-41ec-8765-e32547a68ad5 35 fields · synced May 30, 2026