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Bore Gauge TruSystem 7500 US

FDA UDI

Class II (US FDA UDI)

by NORAS MRI products GmbH

Identity

Trade Name
Bore Gauge TruSystem 7500 US FDA UDI
Generic Name
Skull clamp FDA UDI
Device Name
Collision indicator for transfer during intraoperative brain surgery. FDA UDI
Model / Reference
03 FDA UDI
Description
Collision indicator for transfer during intraoperative brain surgery. FDA UDI

Identifiers

Catalog Number
117899 FDA UDI
Primary DI / UDI-DI
04251269206719 FDA UDI
510(k) Number
K133506 FDA UDI
FDA Product Code
MOS FDA UDI
GMDN Term
Skull clamp 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

Yes

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
MRI Safety
MR Conditional FDA UDI

Category: Skull clamp

Bore Gauge TruSystem 7500 US by NORAS MRI products GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skull clamp.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 654102b5-0b23-4aaf-b0ca-433b890e3ac3 35 fields · synced May 30, 2026