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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
Surgical screwdriver, reusable FDA UDI
Device Name
Short ratchet key for angled screw channel FDA UDI
Model / Reference
MT-ESR10 FDA UDI
Description
Short ratchet key for angled screw channel FDA UDI

Identifiers

Catalog Number
MT-ESR10 FDA UDI
Primary DI / UDI-DI
07290109002644 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Surgical screwdriver, reusable 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: Surgical screwdriver, reusable

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

Similar devices

Also classified as Surgical screwdriver, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7f036bb2-09bc-476a-9e6c-abaa5bc007ce 34 fields · synced May 31, 2026