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Kheiron

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 01TR2120

by S.m.a.i.o

Identity

Trade Name
KHEIRON EUDAMEDFDA UDI
Generic Name
Spinal implant trial FDA UDI
Device Name
Gabarit pour tige L120mm EUDAMED
L120mm rod template FDA UDI
Model / Reference
01TR2120 EUDAMEDFDA UDI
Description
L120mm rod template FDA UDI

Identifiers

Catalog Number
01TR2120 FDA UDI
Primary DI / UDI-DI
03701313002169 EUDAMEDFDA UDI
Basic UDI-DI
B-03701313002169 EUDAMED
FDA Product Code
HWT FDA UDI
EMDN Code
L0999 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Spinal implant trial FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
888.4800 FDA UDI
Market of Registration
France 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Kheiron by S.m.a.i.o — Class I — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
S.m.a.i.o
EUDAMED SRN
FR-MF-000002399

Sources (2)

  • EUDAMED 394ad5fe-03cb-4798-85c9-329f67b36425 61 fields · synced Jul 17, 2026
  • FDA UDI edd4028c-23ee-450f-96fa-85de251d8f46 35 fields · synced May 29, 2026