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Endorectal Coil Holder Repair Kit

FDA UDI

Class II (US FDA UDI)

by RAPID Biomedical GmbH

Identity

Trade Name
Endorectal Coil Holder Repair Kit FDA UDI
Generic Name
MRI system coil, radio-frequency FDA UDI
Device Name
ER Coil Holder Repair Kit FDA UDI
Model / Reference
ZUB-01979 FDA UDI
Description
ER Coil Holder Repair Kit FDA UDI

Identifiers

Catalog Number
none FDA UDI
Primary DI / UDI-DI
04260487680447 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: MRI system coil, radio-frequency

Endorectal Coil Holder Repair Kit by RAPID Biomedical GmbH — 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

Sources (1)

  • FDA UDI df84c1f7-8182-479b-b702-ff5ef266570a 35 fields · synced May 30, 2026