Dr. Brown's

FDA UDI

Class I (US FDA UDI)

by Dr. Brown's Company

Identity

Trade Name: Dr. Brown's FDA UDI
Generic Name: Medicine cup, reusable FDA UDI
Device Name: Healthy Baby Essentials - Pacidose, Aspirator, Cold compress FDA UDI
Model / Reference: HG085 FDA UDI
Description: Healthy Baby Essentials - Pacidose, Aspirator, Cold compress FDA UDI

Identifiers

Primary DI / UDI-DI: 00072239325087 FDA UDI
FDA Product Code: KYX FDA UDI
BSY FDA UDI
IME FDA UDI
GMDN Term: Medicine cup, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.6430 FDA UDI
868.6810 FDA UDI
890.5700 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Hot/cold therapy pack, reusable Medicine cup, reusable Nasal aspirator, manual

Dr. Brown's by Dr. Brown's Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Dr. Brown's Company

Sources (1)

FDA UDI 7f87e6a8-0e41-4e37-84ea-7dc3d324299f 33 fields · synced Jun 8, 2026