← Back to catalogue

Winx®

FDA UDI

Class II (US FDA UDI)

by Apnicure, Inc.

Identity

Trade Name
Winx® FDA UDI
Generic Name
General-purpose suction system, line-powered FDA UDI
Device Name
Winx Warranty Console FDA UDI
Model / Reference
A1015-00 FDA UDI
Description
Winx Warranty Console FDA UDI

Identifiers

Catalog Number
A1015-00 FDA UDI
Primary DI / UDI-DI
00852126007544 FDA UDI
FDA Product Code
OZR FDA UDI
GMDN Term
General-purpose suction system, line-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.5570 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General-purpose suction system, line-powered

Winx® by Apnicure, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose suction system, line-powered.

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

Manufacturer
Apnicure, Inc.

Sources (1)

  • FDA UDI 113ad5ff-e00f-4158-a6e3-7818a26d3ce1 35 fields · synced May 29, 2026