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AMSure® Oxygen Mask

FDA UDI

Class I (US FDA UDI)

by Amsino International, Inc.

Identity

Trade Name
AMSure® Oxygen Mask FDA UDI
Generic Name
Nebulizing system delivery set, single-use FDA UDI
Device Name
AMSure® Oxygen Mask Pediatric Standard Medium Concentration with 7 ft Star Tubing FDA UDI
Model / Reference
1 FDA UDI
Description
AMSure® Oxygen Mask Pediatric Standard Medium Concentration with 7 ft Star Tubing FDA UDI

Identifiers

Catalog Number
AS74030 FDA UDI
Primary DI / UDI-DI
10704411009559 FDA UDI
FDA Product Code
BYG FDA UDI
GMDN Term
Nebulizing system delivery set, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5580 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

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: Nebulizing system delivery set, single-use

AMSure® Oxygen Mask by Amsino International, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nebulizing system delivery set, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 80a4e8a8-7d77-44e8-a461-6f41efa0bf17 34 fields · synced Jun 8, 2026