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Nezzie Junior

FDA UDI

Class I (US FDA UDI)

by Blickman Industries LLC

Identity

Trade Name
Nezzie Junior FDA UDI
Generic Name
Handgrip disability-assistive walker, non-powered, non-foldable FDA UDI
Device Name
Nezzie Junior Ambulation Device FDA UDI
Model / Reference
NZ9100 FDA UDI
Description
Nezzie Junior Ambulation Device FDA UDI

Identifiers

Catalog Number
0429100000 FDA UDI
Primary DI / UDI-DI
00850038811990 FDA UDI
FDA Product Code
LHC FDA UDI
GMDN Term
Handgrip disability-assistive walker, non-powered, non-foldable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5950 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 Junior 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 8e30e108-3e07-4d29-b2a8-9dea11b6b346 34 fields · synced Jun 8, 2026