← Back to catalogue

Ulnar Nerve Protector

FDA UDI

Class I (US FDA UDI)

by Walgreen Health Solutions, LLC

Identity

Trade Name
ULNAR NERVE PROTECTOR FDA UDI
Generic Name
Arm friction/impact protector FDA UDI
Device Name
ULNAR NERVE PROTECTOR, Arm Friction/Impact Protector, One Size, Set of 2 FDA UDI
Model / Reference
831727001663 FDA UDI
Description
ULNAR NERVE PROTECTOR, Arm Friction/Impact Protector, One Size, Set of 2 FDA UDI

Identifiers

Catalog Number
831727001663 FDA UDI
Primary DI / UDI-DI
G0648317270016631 FDA UDI
FDA Product Code
FMP FDA UDI
GMDN Term
Arm friction/impact protector FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6450 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Arm friction/impact protector

Ulnar Nerve Protector by Walgreen Health Solutions, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Arm friction/impact protector.

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 34e73cf2-0ee5-4b54-b8d7-58da1f34ed62 35 fields · synced Jun 8, 2026