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22mm Smoothbore Exhalation Valve Breathing System With Monitoring Line 1.6m

FDA UDI

Class II (US FDA UDI)

by Intersurgical Incorporated

Identity

Trade Name
22MM SMOOTHBORE EXHALATION VALVE BREATHING SYSTEM WITH MONITORING LINE 1.6M FDA UDI
Generic Name
Ventilator breathing circuit, reusable FDA UDI
Device Name
22MM SMOOTHBORE EXHALATION VALVE BREATHING SYSTEM WITH MONITORING LINE 1.6M FDA UDI
Model / Reference
5183000 FDA UDI
Description
22MM SMOOTHBORE EXHALATION VALVE BREATHING SYSTEM WITH MONITORING LINE 1.6M FDA UDI

Identifiers

Primary DI / UDI-DI
05030267069750 FDA UDI
510(k) Number
K132143 FDA UDI
FDA Product Code
CBP FDA UDI
GMDN Term
Ventilator breathing circuit, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5870 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

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, reusable

22mm Smoothbore Exhalation Valve Breathing System With Monitoring Line 1.6m by Intersurgical Incorporated — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Ventilator breathing circuit, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 857abc80-6002-4a59-99cf-17485830801c 35 fields · synced May 30, 2026