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Mis

FDA UDI

Class I (US FDA UDI)

by MIS Implants Technologies Ltd.

Identity

Trade Name
MIS FDA UDI
Generic Name
Screwing power tool attachment FDA UDI
Device Name
MGUIDE motor insertion tool, coni. con., V3, NP FDA UDI
Model / Reference
VG-GMN10 FDA UDI
Description
MGUIDE motor insertion tool, coni. con., V3, NP FDA UDI

Identifiers

Catalog Number
VG-GMN10 FDA UDI
Primary DI / UDI-DI
07290109015262 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Screwing power tool attachment FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Screwing power tool attachment

Mis by MIS Implants Technologies Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Screwing power tool attachment.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI dda013cc-e976-44ad-8848-6bfc98c3bcae 34 fields · synced May 31, 2026