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Spine Coil N.10

FDA UDI

Class II (US FDA UDI)

by Esaote

Identity

Trade Name
SPINE COIL N.10 FDA UDI
Generic Name
MRI system coil, radio-frequency FDA UDI
Device Name
Coil for G-scan / S-scan FDA UDI
Model / Reference
9103050000 FDA UDI
Description
Coil for G-scan / S-scan FDA UDI

Identifiers

Primary DI / UDI-DI
08056304452474 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

Yes

FDA UDI

Category: MRI system coil, radio-frequency

Spine Coil N.10 by Esaote — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as MRI system coil, radio-frequency.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Esaote

Sources (1)

  • FDA UDI 16bf44fe-72f7-4e91-a7ac-4a9e33cccef4 33 fields · synced May 30, 2026