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Inflexion IMRIS Universal HFF

EUDAMEDFDA UDI

Class I (EU MDR)

Ref CP-INHFF-232-01

by ClearPoint Neuro, Inc.

Identity

Trade Name
Inflexion IMRIS Universal HFF EUDAMED
ClearPoint FDA UDI
Generic Name
Skull clamp FDA UDI
Device Name
ClearPoint Inflexion EUDAMED
ClearPoint Inflexion IMRIS Universal HFF FDA UDI
Model / Reference
CP-INHFF-232-01 EUDAMEDFDA UDI
Description
ClearPoint Inflexion IMRIS Universal HFF FDA UDI

Identifiers

Catalog Number
CP-INHFF-232-01 FDA UDI
Primary DI / UDI-DI
00850376007505 EUDAMEDFDA UDI
Basic UDI-DI
0850376007488J EUDAMED
Direct Marketing DI
00850376007505 EUDAMED
510(k) Number
K191701 FDA UDI
FDA Product Code
HBL FDA UDI
EMDN Code
Z12100680 STEREOTACTIC NEUROSURGERY INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Skull clamp FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
882.4460 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Inflexion IMRIS Universal HFF by Clearpoint Neuro, Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
US-MF-000010239
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED 75a1dccf-0407-4a3b-8ef1-3ac309fb23a9 61 fields · synced Jun 18, 2026
  • FDA UDI 29a0694d-648c-43b4-ade9-00da682d3ad4 36 fields · synced May 30, 2026