ANEclear

FDA UDI

Class I (US FDA UDI)

by Anecare Llc

Identity

Trade Name: ANEclear FDA UDI
Generic Name: Anaesthesia workstation gas scavenger FDA UDI
Device Name: Anesthesia Recovery Device FDA UDI
Model / Reference: 2 FDA UDI
Description: Anesthesia Recovery Device FDA UDI

Identifiers

Catalog Number: 90020 FDA UDI
Primary DI / UDI-DI: 00863034000329 FDA UDI
510(k) Number: K033028 FDA UDI
FDA Product Code: BYW FDA UDI
CBN FDA UDI
GMDN Term: Anaesthesia workstation gas scavenger FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 868.5675 FDA UDI
868.5430 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

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Anaesthesia workstation gas scavenger

ANEclear by Anecare Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: Anecare Llc

Sources (1)

FDA UDI f3124d40-d5cd-48f9-bb4c-6ce48fa33cea 36 fields · synced May 30, 2026