← Back to catalogue

Safety 1st

FDA UDI

Class I (US FDA UDI)

by Dorel Juvenile Group, Inc.

Identity

Trade Name
Safety 1st FDA UDI
Generic Name
Nasal aspirator, manual FDA UDI
Device Name
Baby on Board Health Kit FDA UDI
Model / Reference
IH594 FDA UDI
Description
Baby on Board Health Kit FDA UDI

Identifiers

Primary DI / UDI-DI
10884392951075 FDA UDI
FDA Product Code
KYZ FDA UDI
KYX FDA UDI
FLL FDA UDI
LRJ FDA UDI
EFW FDA UDI
GMDN Term
Nasal aspirator, manual FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6960 FDA UDI
880.6430 FDA UDI
880.2910 FDA UDI
880.6890 FDA UDI
872.6855 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

No

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthodontic pliersIntermittent electronic patient thermometerBasic manual toothbrushVial/bottle adaptor, non-hermetic

Safety 1st by Dorel Juvenile Group, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose syringe, reusable.

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
Dorel Juvenile Group, Inc.

Sources (1)

  • FDA UDI 4013613f-06cb-40a3-bda2-bd237a1b37c4 33 fields · synced May 30, 2026