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Avazzia

FDA UDI

Class II (US FDA UDI)

by Avazzia, Inc.

Identity

Trade Name
Avazzia FDA UDI
Generic Name
Transcutaneous electrical stimulation lead FDA UDI
Device Name
Lead Wire, 250-RB FDA UDI
Model / Reference
AA-LW-250-RB FDA UDI
Description
Lead Wire, 250-RB FDA UDI

Identifiers

Catalog Number
AA-LW-250-RB FDA UDI
Primary DI / UDI-DI
00851530007416 FDA UDI
FDA Product Code
IKD FDA UDI
GMDN Term
Transcutaneous electrical stimulation lead FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.1175 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: Transcutaneous electrical stimulation lead

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

Similar devices

Also classified as Transcutaneous electrical stimulation lead.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Avazzia, Inc.

Sources (1)

  • FDA UDI a535d8d9-bbdb-4087-a517-26201d9571be 34 fields · synced May 30, 2026