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Extraction Screw

FDA UDI

Class I (US FDA UDI)

by Noris Medical Ltd

Identity

Trade Name
Extraction Screw FDA UDI
Generic Name
Surgical screwdriver, reusable FDA UDI
Device Name
EZguide, Extraction Screw, Short, CP, Ti. FDA UDI
Model / Reference
NMCX2860 FDA UDI
Description
EZguide, Extraction Screw, Short, CP, Ti. FDA UDI

Identifiers

Catalog Number
NMCX2860 FDA UDI
Primary DI / UDI-DI
07290116153643 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

Yes

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical screwdriver, reusable

Extraction Screw by Noris Medical 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

Manufacturer
Noris Medical Ltd

Sources (1)

  • FDA UDI 1c388a98-e1e4-4399-9715-bbd7b66fd89a 35 fields · synced May 31, 2026