Philips

FDA UDI

Class II (US FDA UDI)

by Shanghai Chenguang Medical Technologies Co., Ltd

Identity

Trade Name: Philips FDA UDI
Generic Name: MRI system coil, radio-frequency FDA UDI
Device Name: Quad Head Coil 1.5T FDA UDI
Model / Reference: 4522-133-17271 FDA UDI
Description: Quad Head Coil 1.5T FDA UDI

Identifiers

Primary DI / UDI-DI: 06970564410215 FDA UDI
FDA Product Code: MOS FDA UDI
GMDN Term: MRI system coil, radio-frequency FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 892.1000 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

MRI Safety

MR Safe FDA UDI

Category: MRI system coil, radio-frequency

Philips by Shanghai Chenguang Medical Technologies Co., Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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ScanMed Long Bone (L) Coil — SCANMED, LLC · 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: Shanghai Chenguang Medical Technologies Co., Ltd

Sources (1)

FDA UDI 7cf3ab40-956a-472d-b658-499709301245 33 fields · synced May 30, 2026