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Kheiron

FDA UDIEUDAMED

Class I (US FDA UDI)

by S.m.a.i.o

Identity

Trade Name
KHEIRON FDA UDI
Generic Name
Surgical screwdriver, reusable FDA UDI
Device Name
Large Hudson pedicle screwdriver FDA UDI
Model / Reference
01DS2024 FDA UDI
Description
Large Hudson pedicle screwdriver FDA UDI

Identifiers

Catalog Number
01DS2024 FDA UDI
Primary DI / UDI-DI
03701313009366 FDA UDI
FDA Product Code
HXX FDA UDI
GMDN Term
Surgical screwdriver, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Category: Surgical screwdriver, reusable

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

Similar devices

Also classified as Surgical screwdriver, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
S.m.a.i.o

Sources (2)

  • FDA UDI b2191810-a0e8-472c-90c7-03e74f9e57c4 35 fields · synced Jun 20, 2026
  • EUDAMED 1 fields · synced May 28, 2026