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Soft Sock ®

FDA UDI

Class II (US FDA UDI)

by Knit-Rite, Inc

Identity

Trade Name
SOFT SOCK ® FDA UDI
Generic Name
Compression/pressure sock/stocking, single-use FDA UDI
Device Name
SOFT SOCK 3PLY X-STATIC RGXS FITS SIZE #1, #2 X 8-12 FDA UDI
Model / Reference
1SX3RGXS FDA UDI
Description
SOFT SOCK 3PLY X-STATIC RGXS FITS SIZE #1, #2 X 8-12 FDA UDI

Identifiers

Catalog Number
1SX3RGXS FDA UDI
Primary DI / UDI-DI
00674854000969 FDA UDI
FDA Product Code
DWL FDA UDI
FQL FDA UDI
GMDN Term
Compression/pressure sock/stocking, single-use FDA UDI

Classification

Device Class
Class II 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

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: Compression/pressure sock/stocking, single-use

Soft Sock ® by Knit-Rite, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Compression/pressure sock/stocking, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Knit-Rite, Inc

Sources (1)

  • FDA UDI 32235c0f-c1d3-4eb2-8910-923cc5d01d8f 34 fields · synced Jun 8, 2026