← Back to catalogue

Shin Neoprene Sleeve

FDA UDI

Class I (US FDA UDI)

by AliMed, LLC

Identity

Trade Name
SHIN NEOPRENE SLEEVE FDA UDI
Generic Name
Calf/shin orthosis FDA UDI
Model / Reference
66295/NA/NA/SM FDA UDI

Identifiers

Catalog Number
2970006101 FDA UDI
Primary DI / UDI-DI
00733657247916 FDA UDI
FDA Product Code
IQI FDA UDI
GMDN Term
Calf/shin orthosis FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3475 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

Yes

FDA UDI

Category: Calf/shin orthosis

Shin Neoprene Sleeve by AliMed, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Calf/shin orthosis.

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

Manufacturer
AliMed, LLC

Sources (1)

  • FDA UDI d13c1f52-24fd-4920-a063-ca6bf89eaf72 34 fields · synced Jun 9, 2026