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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
Bone trephine, reusable FDA UDI
Device Name
Trephine bur 6mm FDA UDI
Model / Reference
MT-00600 FDA UDI
Description
Trephine bur 6mm FDA UDI

Identifiers

Catalog Number
MT-00600 FDA UDI
Primary DI / UDI-DI
07290109009483 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Bone trephine, 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: Bone trephine, reusable

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

Similar devices

Also classified as Bone trephine, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 92d1112f-2efe-47cf-b5e5-bcd71f6a97d5 34 fields · synced May 31, 2026