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icotec Lumbar Cage In-line Handle

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 38-026Model In-line Handle

by icotec ag

Identity

Trade Name
icotec Lumbar Cage In-line Handle EUDAMED
icotec Lumbar Cage, In-Line Handle FDA UDI
Generic Name
Surgical instrument handle, non-torque-limiting FDA UDI
Device Name
icotec Lumbar Cage, In-Line Handle FDA UDI
Model / Reference
In-line Handle EUDAMED
38-026 EUDAMEDFDA UDI
Description
icotec Lumbar Cage, In-Line Handle FDA UDI

Identifiers

Catalog Number
38-026 FDA UDI
Primary DI / UDI-DI
07640164841700 EUDAMEDFDA UDI
Basic UDI-DI
764017255iLCAGE00048B EUDAMED
Direct Marketing DI
07640164841700 EUDAMED
FDA Product Code
MAX FDA UDI
ODP FDA UDI
EMDN Code
L1109 NEUROSURGERY AND SPINAL SURGERY INSTRUMENT KITS, REUSABLE EUDAMED
GMDN Term
Surgical instrument handle, non-torque-limiting FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
888.3080 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

No

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Device sterilization/disinfection container, reusable

icotec Lumbar Cage In-line Handle by icotec AG — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
icotec ag
EUDAMED SRN
CH-MF-000026833
Authorised Representative
icotec Medical GmbH DE-AR-000016837

Sources (2)

  • EUDAMED 7242a6dc-1cdf-4764-ba92-5e018ce95ec1 61 fields · synced Jun 19, 2026
  • FDA UDI ccf195df-2fba-42e1-9872-d1dbd5699a4f 35 fields · synced May 30, 2026