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Health Support

FDA UDI

Class I (US FDA UDI)

by Carolon Co.

Identity

Trade Name
Health Support FDA UDI
Generic Name
Compression/pressure sock/stocking, reusable FDA UDI
Model / Reference
Thigh FDA UDI

Identifiers

Primary DI / UDI-DI
00078301312023 FDA UDI
FDA Product Code
FQL FDA UDI
GMDN Term
Compression/pressure sock/stocking, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5780 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Compression/pressure sock/stocking, reusable

Health Support by Carolon Co. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Compression/pressure sock/stocking, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Carolon Co.

Sources (1)

  • FDA UDI 14123289-8c69-4e5a-b3a4-557d240f7058 32 fields · synced May 30, 2026