Scancoat

FDA UDI

Class II (US FDA UDI)

by Domico Med-Device, Llc

Identity

Trade Name: SCANCOAT FDA UDI
Generic Name: Radiological general body-part positioner FDA UDI
Device Name: PAD, PEDIATRIC POSITIONING FDA UDI
Model / Reference: 9020F FDA UDI
Description: PAD, PEDIATRIC POSITIONING FDA UDI

Identifiers

Primary DI / UDI-DI: 00810050241441 FDA UDI
FDA Product Code: KXJ FDA UDI
CCX FDA UDI
GMDN Term: Radiological general body-part positioner FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 892.1980 FDA UDI
868.6820 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Radiological general body-part positioner

Scancoat by Domico Med-Device, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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AADCO — AADCO MEDICAL, INC. · Class I
Oakworks Medical — OAKWORKS, 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: Domico Med-Device, Llc

Sources (1)

FDA UDI a45c38c3-2b16-4d29-a925-8b6a87bf371e 33 fields · synced Jun 7, 2026