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DORO LUCENT® iMRI Transfer Collision Indicator

FDA UDI

Class II (US FDA UDI)

by pro med instruments GmbH, Herstellung und Vertrieb medizinisch technischer Ausrüstung

Identity

Trade Name
DORO LUCENT® iMRI Transfer Collision Indicator FDA UDI
Generic Name
Skull clamp FDA UDI
Device Name
DORO LUCENT® iXI Transfer Collision Indicator to SIEMENS Cam FDA UDI
Model / Reference
4003.533 FDA UDI
Description
DORO LUCENT® iXI Transfer Collision Indicator to SIEMENS Cam FDA UDI

Identifiers

Primary DI / UDI-DI
04250435536117 FDA UDI
FDA Product Code
HBL FDA UDI
GMDN Term
Skull clamp FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4460 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

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Skull clamp

DORO LUCENT® iMRI Transfer Collision Indicator by pro med instruments GmbH, Herstellung und Vertrieb medizinisch technischer Ausrüstung — Class II — FDA UDI…

Similar devices

Also classified as Skull clamp.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
pro med instruments GmbH, Herstellung und Vertrieb medizinisch technischer Ausrüstung

Sources (1)

  • FDA UDI d07f55bb-1861-4c42-9c15-ad10428c2b5e 33 fields · synced May 30, 2026