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Safety 1st

FDA UDI

Class I (US FDA UDI)

by Dorel Juvenile Group, Inc.

Identity

Trade Name
Safety 1st FDA UDI
Generic Name
Oral medicine dropper FDA UDI
Device Name
Home From the Hospital Kit FDA UDI
Model / Reference
IH576 FDA UDI
Description
Home From the Hospital Kit FDA UDI

Identifiers

Primary DI / UDI-DI
20884392950495 FDA UDI
FDA Product Code
KYX FDA UDI
FLL FDA UDI
LRJ FDA UDI
KYZ FDA UDI
GMDN Term
Oral medicine dropper FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6430 FDA UDI
880.2910 FDA UDI
880.6890 FDA UDI
880.6960 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: Intermittent electronic patient thermometerSkin cleaning wipeNasal aspirator, manualOral medicine dropper

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

Similar devices

Also classified as Oral medicine dropper.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3e299ba6-c318-47d6-bae3-d2da8eb0e0a0 33 fields · synced Jun 8, 2026