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Endure Industries

FDA UDI

Class I (US FDA UDI)

by Endure Industries, Inc.

Identity

Trade Name
ENDURE INDUSTRIES FDA UDI
Generic Name
Suction system catheter, general-purpose FDA UDI
Device Name
Sterile non-woven sponge (40g, 4*4, 4ply) FDA UDI
Model / Reference
WSS44 FDA UDI
Description
Sterile non-woven sponge (40g, 4*4, 4ply) FDA UDI

Identifiers

Catalog Number
WSS44 FDA UDI
Primary DI / UDI-DI
00840118609715 FDA UDI
FDA Product Code
NAB FDA UDI
GMDN Term
Suction system catheter, general-purpose FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4014 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Suction system catheter, general-purpose

Endure Industries by Endure Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suction system catheter, general-purpose.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e5094574-d8d9-4f33-8b8b-a6c9f95bbf22 36 fields · synced May 30, 2026