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Medyssey Navigation Instrument

FDA UDI

Class II (US FDA UDI)

by Medyssey Co., Ltd.

Identity

Trade Name
Medyssey Navigation Instrument FDA UDI
Generic Name
Surgical screwdriver, reusable FDA UDI
Device Name
Iliad Navigation Screw driver FDA UDI
Model / Reference
SNNPD-N01 FDA UDI
Description
Iliad Navigation Screw driver FDA UDI

Identifiers

Primary DI / UDI-DI
08809974444382 FDA UDI
510(k) Number
K242806 FDA UDI
FDA Product Code
NKB FDA UDI
OLO FDA UDI
GMDN Term
Surgical screwdriver, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 FDA UDI
882.4560 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

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: Surgical screwdriver, reusable

Medyssey Navigation Instrument by Medyssey Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical screwdriver, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medyssey Co., Ltd.

Sources (1)

  • FDA UDI 7a12fd19-8905-483a-a00c-875a6409dc29 34 fields · synced Jun 8, 2026