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AngelMed Guardian Programmer USB Flash Drive

FDA UDI

Class III (US FDA UDI)

by Avertix Medical Inc.

Identity

Trade Name
AngelMed Guardian Programmer USB Flash Drive FDA UDI
Generic Name
Implantable cardiac device management application software FDA UDI
Device Name
PROG-003 USB Flash Drive FDA UDI
Model / Reference
0204-2100-077#P10 FDA UDI
Description
PROG-003 USB Flash Drive FDA UDI

Identifiers

Catalog Number
0204-2100-077#P10 FDA UDI
Primary DI / UDI-DI
00850012625124 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

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

No

FDA UDI

Category: Implantable cardiac device management application software

AngelMed Guardian Programmer USB Flash Drive 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 f280e39f-31d6-498e-be8a-b4e46d0c6f9b 35 fields · synced May 30, 2026