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HeelShield

FDA UDI

Class I (US FDA UDI)

by Primo Inc

Identity

Trade Name
HeelShield FDA UDI
Generic Name
Heel protector FDA UDI
Device Name
HS51S HeelShield - Small 12/each; HS51SW HeelShield w/wedge - Small 8/each FDA UDI
Model / Reference
HS51S FDA UDI
Description
HS51S HeelShield - Small 12/each; HS51SW HeelShield w/wedge - Small 8/each FDA UDI

Identifiers

Catalog Number
HS51S, HS51SW FDA UDI
Primary DI / UDI-DI
00810006680539 FDA UDI
FDA Product Code
FMP FDA UDI
GMDN Term
Heel 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Heel protector

HeelShield by Primo Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Heel protector.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Primo Inc

Sources (1)

  • FDA UDI b5a88923-4e9e-4b1c-a914-bf5e52635f85 34 fields · synced May 30, 2026