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Kheiron

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 01RN5010

by S.m.a.i.o

Identity

Trade Name
KHEIRON EUDAMEDFDA UDI
Generic Name
Surgical screwdriver, reusable FDA UDI
Device Name
Tourne-écrou 9mm EUDAMED
9mm nut driver FDA UDI
Model / Reference
01RN5010 EUDAMEDFDA UDI
Description
9mm nut driver FDA UDI

Identifiers

Catalog Number
01RN5010 FDA UDI
Primary DI / UDI-DI
03701313002756 EUDAMEDFDA UDI
Basic UDI-DI
B-03701313002756 EUDAMED
FDA Product Code
LXH FDA UDI
EMDN Code
L0999 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Surgical screwdriver, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
888.4540 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 7320be50-e871-4a02-bfe9-3c572dee1e8b 61 fields · synced Jul 27, 2026
  • FDA UDI c53f0fc5-ddd2-41a7-b76a-1f052101de0d 35 fields · synced May 30, 2026