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AMSure® Closed Suction System For Neonates/pediatrics

FDA UDI

Class I (US FDA UDI)

by Amsino International, Inc.

Identity

Trade Name
AMSure® Closed Suction System For Neonates/pediatrics FDA UDI
Generic Name
Airway suction catheter FDA UDI
Device Name
5Fr •Closed Suction Catheter •2.0,2.5 mm Y-Adapters •Day Sticker FDA UDI
Model / Reference
1 FDA UDI
Description
5Fr •Closed Suction Catheter •2.0,2.5 mm Y-Adapters •Day Sticker FDA UDI

Identifiers

Catalog Number
VS360RC24 FDA UDI
Primary DI / UDI-DI
10704411018063 FDA UDI
FDA Product Code
BSY FDA UDI
GMDN Term
Airway suction catheter FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6810 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Category: Airway suction catheter

AMSure® Closed Suction System For Neonates/pediatrics by Amsino International, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Airway suction catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1c956999-f9dd-42d7-9e2e-2a3df7ee838d 34 fields · synced May 30, 2026