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Nezzie

FDA UDI

Class I (US FDA UDI)

by Blickman Industries LLC

Identity

Trade Name
Nezzie FDA UDI
Generic Name
Handgrip disability-assistive walker, non-powered, non-foldable FDA UDI
Device Name
Nezzie Ambulation Device FDA UDI
Model / Reference
NZ9000 FDA UDI
Description
Nezzie Ambulation Device FDA UDI

Identifiers

Catalog Number
0429000000 FDA UDI
Primary DI / UDI-DI
00850038811983 FDA UDI
FDA Product Code
ITJ FDA UDI
GMDN Term
Handgrip disability-assistive walker, non-powered, non-foldable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3825 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Handgrip disability-assistive walker, non-powered, non-foldable

Nezzie by Blickman Industries LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Handgrip disability-assistive walker, non-powered, non-foldable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Blickman Industries LLC

Sources (1)

  • FDA UDI f4bb0d90-70c2-4748-a53f-477c38f93499 34 fields · synced Jun 8, 2026