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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
Hot/cold therapy pack, reusable FDA UDI
Device Name
Gripebelt with teether FDA UDI
Model / Reference
HG103 FDA UDI
Description
Gripebelt with teether FDA UDI

Identifiers

Primary DI / UDI-DI
00072239321294 FDA UDI
FDA Product Code
IME FDA UDI
MEF FDA UDI
GMDN Term
Hot/cold therapy pack, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5700 FDA UDI
872.5550 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Hot/cold therapy pack, reusableInfant care kit

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

Similar devices

Also classified as Infant care kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dr. Brown's Company

Sources (1)

  • FDA UDI cf697374-7b99-4e1b-a7c1-3ab3a6a020f2 33 fields · synced Jun 8, 2026