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30mm UniFlow coaxial breathing system with 0.5m limb, 2.4m

FDA UDI

Class I (US FDA UDI)

by Intersurgical Incorporated

Identity

Trade Name
30mm UniFlow coaxial breathing system with 0.5m limb, 2.4m FDA UDI
Generic Name
Anaesthesia breathing circuit, reusable FDA UDI
Device Name
30mm UniFlow coaxial breathing system with 0.5m limb, 2.4m FDA UDI
Model / Reference
29016000 FDA UDI
Description
30mm UniFlow coaxial breathing system with 0.5m limb, 2.4m FDA UDI

Identifiers

Primary DI / UDI-DI
00816472023009 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

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
MRI Safety
MR Safe FDA UDI

Category: Anaesthesia breathing circuit, reusable

30mm UniFlow coaxial breathing system with 0.5m limb, 2.4m by Intersurgical Incorporated — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Anaesthesia breathing circuit, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bcc87cd4-35e4-4d00-a271-cab8c4e4c98d 34 fields · synced Jun 1, 2026