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8 channel wrist coil

FDA UDI

Class II (US FDA UDI)

by Siemens Shenzhen Magnetic Resonance Ltd.

Identity

Trade Name
8 channel wrist coil FDA UDI
Generic Name
Full-body MRI system, superconducting magnet FDA UDI
Device Name
MRI Coil FDA UDI
Model / Reference
10352487 FDA UDI
Description
MRI Coil FDA UDI

Identifiers

Primary DI / UDI-DI
04056869038964 FDA UDI
FDA Product Code
LNH FDA UDI
GMDN Term
Full-body MRI system, superconducting magnet 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

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Full-body MRI system, superconducting magnet

8 channel wrist coil by Siemens Shenzhen Magnetic Resonance Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Full-body MRI system, superconducting magnet.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4c2e5ea4-d6f2-4532-8124-be50ee5eea04 34 fields · synced May 30, 2026