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icotec Lumbar Cage T-Handle

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 38-025Model T-Handle

by icotec ag

Identity

Trade Name
icotec Lumbar Cage T-Handle EUDAMED
icotec Lumbar Cage, T-Handle FDA UDI
Generic Name
Surgical instrument handle, non-torque-limiting FDA UDI
Device Name
icotec Lumbar Cage, T-Handle FDA UDI
Model / Reference
T-Handle EUDAMED
38-025 EUDAMEDFDA UDI
Description
icotec Lumbar Cage, T-Handle FDA UDI

Identifiers

Catalog Number
38-025 FDA UDI
Primary DI / UDI-DI
07640164841656 EUDAMEDFDA UDI
Basic UDI-DI
764017255iLCAGE000389 EUDAMED
Direct Marketing DI
07640164841656 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 T-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 0743e941-d428-4081-9685-a34438bd6335 61 fields · synced Jul 10, 2026
  • FDA UDI 5b71af89-02a9-47e4-8bac-c7185517fc49 35 fields · synced May 30, 2026