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Anesthesia Breathing Circuit Kit

FDA UDI

Class I (US FDA UDI)

by Typenex Medical, LLC

Identity

Trade Name
Anesthesia Breathing Circuit Kit FDA UDI
Generic Name
Anaesthesia breathing circuit, single-use FDA UDI
Device Name
Adult Anesthesia Breathing Circuit Kit - 90" Dual Limb Breathing Circuit - Bacterial Viral Filter - Size 5 Anesthesia Mask - 3L Breathing Bag - 10 ft Gas Sampling Line FDA UDI
Model / Reference
KB0101A FDA UDI
Description
Adult Anesthesia Breathing Circuit Kit - 90" Dual Limb Breathing Circuit - Bacterial Viral Filter - Size 5 Anesthesia Mask - 3L Breathing Bag - 10 ft Gas Sampling Line FDA UDI

Identifiers

Primary DI / UDI-DI
06941850890271 FDA UDI
FDA Product Code
OFP FDA UDI
GMDN Term
Anaesthesia 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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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, single-use

Anesthesia Breathing Circuit Kit by Typenex Medical, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anaesthesia 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 e7edd9f7-7342-4861-a852-285ea24aee85 34 fields · synced Jun 8, 2026