Child insert for chair

FDA UDI

Class II (US FDA UDI)

by Megin Oy

Identity

Trade Name: Child insert for chair FDA UDI
Generic Name: Electroencephalograph FDA UDI
Device Name: A booster seat and neck collar for pediatric patients. FDA UDI
Model / Reference: BC20899N FDA UDI
Description: A booster seat and neck collar for pediatric patients. FDA UDI

Identifiers

Primary DI / UDI-DI: 06430056480077 FDA UDI
FDA Product Code: OLY FDA UDI
GMDN Term: Electroencephalograph FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 882.1400 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

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Electroencephalograph

Child insert for chair by Megin Oy — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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WR19 — ZETO INC · Class II

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 II	Pending data

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Manufacturer

Manufacturer: Megin Oy

Sources (1)

FDA UDI b034698d-2f4c-4ec2-841e-b3e5ddd70eab 33 fields · synced Jun 8, 2026