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Endure Industries

FDA UDI

Class II (US FDA UDI)

by Endure Industries, Inc.

Identity

Trade Name
ENDURE INDUSTRIES FDA UDI
Generic Name
Anaesthesia breathing circuit, single-use FDA UDI
Device Name
Expandable Breathing Circuit Adult 71" FDA UDI
Model / Reference
BGE73 FDA UDI
Description
Expandable Breathing Circuit Adult 71" FDA UDI

Identifiers

Catalog Number
BGE73 FDA UDI
Primary DI / UDI-DI
00840118609999 FDA UDI
FDA Product Code
CAH FDA UDI
GMDN Term
Anaesthesia breathing circuit, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5260 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

No

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: Anaesthesia breathing circuit, single-use

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

Similar devices

Also classified as Anaesthesia breathing circuit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c2c6f159-120e-4672-a69a-1d129afbabdf 36 fields · synced May 31, 2026