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Avazzia

FDA UDI

Class I (US FDA UDI)

by Avazzia, Inc.

Identity

Trade Name
Avazzia FDA UDI
Generic Name
Electrode/transducer strap, reusable FDA UDI
Device Name
Wrap, Arm/Leg FDA UDI
Model / Reference
AA-W-Arm Leg FDA UDI
Description
Wrap, Arm/Leg FDA UDI

Identifiers

Catalog Number
AA-W-Arm Leg FDA UDI
Primary DI / UDI-DI
00851530007355 FDA UDI
FDA Product Code
MDR FDA UDI
GMDN Term
Electrode/transducer strap, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5160 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

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrode/transducer strap, reusable

Avazzia by Avazzia, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrode/transducer strap, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Avazzia, Inc.

Sources (1)

  • FDA UDI 0711512f-1284-437d-9209-f330a8b2a12a 34 fields · synced Jun 1, 2026