Smoothbore circuit, 22mm

FDA UDI

Class I (US FDA UDI)

by Intersurgical Incorporated

Identity

Trade Name: Smoothbore circuit, 22mm FDA UDI
Generic Name: Anaesthesia breathing circuit, reusable FDA UDI
Device Name: Smoothbore circuit, 22mm FDA UDI
Model / Reference: B0031001 FDA UDI
Description: Smoothbore circuit, 22mm FDA UDI

Identifiers

Primary DI / UDI-DI: 00816472023603 FDA UDI
FDA Product Code: CAI FDA UDI
GMDN Term: Anaesthesia breathing circuit, reusable 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Safe FDA UDI

Category: Anaesthesia breathing circuit, reusable

Smoothbore circuit, 22mm by Intersurgical Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Trulink — SPACELABS HEALTHCARE (WASHINGTON), INC · Class II

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 I	Pending data

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Manufacturer

Manufacturer: Intersurgical Incorporated

Sources (1)

FDA UDI c5391622-acc7-4888-b8c2-b0bf558b278d 34 fields · synced Jun 1, 2026