Gogo®

FDA UDI

Class II (US FDA UDI)

by Knit-Rite, Inc

Identity

Trade Name: GOGO® FDA UDI
Generic Name: Compression/pressure sock/stocking, single-use FDA UDI
Device Name: T-230 10-15 mmHg KNEE HIGH STOCKINGS MEDIUM COCOA FDA UDI
Model / Reference: 23022 FDA UDI
Description: T-230 10-15 mmHg KNEE HIGH STOCKINGS MEDIUM COCOA FDA UDI

Identifiers

Primary DI / UDI-DI: 00721734230227 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Compression/pressure sock/stocking, single-use

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

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

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MEDI — MEDI MANUFACTURING, INC. · Class II
JOBST Relief — BSN MEDICAL, INC. · Class II
VenoTrain micro — Bauerfeind GmbH & Co. · Class II
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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Knit-Rite, Inc

Sources (1)

FDA UDI 6ca91a27-62ac-4700-a928-259293240c7e 33 fields · synced Jun 6, 2026