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22mm Smoothbore System With Leak Port, Monitor Line, For Starmed Helmets

FDA UDI

Class I (US FDA UDI)

by Intersurgical Incorporated

Identity

Trade Name
22MM SMOOTHBORE SYSTEM WITH LEAK PORT, MONITOR LINE, FOR STARMED HELMETS FDA UDI
Generic Name
Ventilator breathing circuit, single-use FDA UDI
Device Name
22MM SMOOTHBORE SYSTEM WITH LEAK PORT, MONITOR LINE, FOR STARMED HELMETS FDA UDI
Model / Reference
5018011 FDA UDI
Description
22MM SMOOTHBORE SYSTEM WITH LEAK PORT, MONITOR LINE, FOR STARMED HELMETS FDA UDI

Identifiers

Primary DI / UDI-DI
05030267137336 FDA UDI
FDA Product Code
CAI FDA UDI
GMDN Term
Ventilator breathing circuit, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5240 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

Yes

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

No

FDA UDI

Category: Ventilator breathing circuit, single-use

22mm Smoothbore System With Leak Port, Monitor Line, For Starmed Helmets by Intersurgical Incorporated — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Ventilator 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 e2417a83-c36e-4388-8612-ad4b97e4cd33 34 fields · synced Jun 8, 2026