← Back to catalogue

Avaline Medical NJ LLC

FDA UDI

Class I (US FDA UDI)

by Avaline Medical NJ Limited Liability Company

Identity

Trade Name
Avaline Medical NJ LLC FDA UDI
Generic Name
Elbow/ankle friction/impact protector FDA UDI
Device Name
Convoluted Foam Heel Protectors FDA UDI
Model / Reference
vkfhp01.2 FDA UDI
Description
Convoluted Foam Heel Protectors FDA UDI

Identifiers

Catalog Number
vkfhp01.2 FDA UDI
Primary DI / UDI-DI
00667605027896 FDA UDI
FDA Product Code
FMP FDA UDI
GMDN Term
Elbow/ankle friction/impact protector FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6450 FDA UDI
Commercial Distribution
Not 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

Yes

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

Avaline Medical NJ LLC by Avaline Medical NJ Limited Liability Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 404d94a9-34c0-4ae0-a45d-505e99660abf 36 fields · synced Jun 8, 2026