← Back to catalogue

inspired™

FDA UDI

Class I (US FDA UDI)

by Vincent Medical Manufacturing Co., Limited

Identity

Trade Name
inspired™ FDA UDI
Generic Name
Anaesthesia breathing circuit, reusable FDA UDI
Device Name
ABS STARTUP KIT, ADULT, REUSABLE, HYTREL,W/ BAG SUPPORT ARM,1.5m, 2L BAG FDA UDI
Model / Reference
2096536-001 FDA UDI
Description
ABS STARTUP KIT, ADULT, REUSABLE, HYTREL,W/ BAG SUPPORT ARM,1.5m, 2L BAG FDA UDI

Identifiers

Primary DI / UDI-DI
14896138001025 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

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

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, reusable

The Anaesthesia breathing circuit, a reusable device designed for general anesthesia, features a map-approved assembly of devices that conducts medical gases from an anesthesia unit to a patient artificial airway. It includes ventilation tubes and connectors typically with a ventilator or ventilation bag, a carbon dioxide absorber, directional valves, adjustable pressure limiting (APL) valves, and more.

Similar devices

Also classified as Anaesthesia breathing circuit, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 51bd613e-e30c-4383-9bbf-802633d8f4d0 33 fields · synced Jul 8, 2026