Go Green Barrier Sleeve

FDA UDI

Class II (US FDA UDI)

by Manamed Llc

Identity

Trade Name: Go Green Barrier Sleeve FDA UDI
Generic Name: Intermittent venous compression system FDA UDI
Device Name: Barrier sleeves to be used with the M-31 Resuable intermittent compression limb sleeve (10 pairs/box) FDA UDI
Model / Reference: M-32 FDA UDI
Description: Barrier sleeves to be used with the M-31 Resuable intermittent compression limb sleeve (10 pairs/box) FDA UDI

Identifiers

Catalog Number: M-32 FDA UDI
Primary DI / UDI-DI: 00850998008867 FDA UDI
FDA Product Code: JOW FDA UDI
GMDN Term: Intermittent venous compression system FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.5800 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

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Intermittent venous compression system

Go Green Barrier Sleeve by Manamed Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: Manamed Llc

Sources (1)

FDA UDI f7dc1aa7-2793-41d3-b8dc-fd4efb08a6a3 35 fields · synced May 31, 2026