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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
Cushion Foot Sock Knee FDA UDI

Identifiers

Catalog Number
281204 FDA UDI
Primary DI / UDI-DI
00783014281244 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
Not 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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Carolon Co.

Sources (1)

  • FDA UDI 49bf2cb6-c731-452b-b3c6-2e493889e20a 34 fields · synced Jun 1, 2026