← Back to catalogue

Countersink

FDA UDI

Class I (US FDA UDI)

by Megagen Implant Co. Ltd

Identity

Trade Name
Countersink FDA UDI
Generic Name
Fixture/appliance dental drill bit, reusable FDA UDI
Device Name
EZ Plus Ø3.3/ Small FDA UDI
Model / Reference
MCS330N FDA UDI
Description
EZ Plus Ø3.3/ Small FDA UDI

Identifiers

Catalog Number
MCS330N FDA UDI
Primary DI / UDI-DI
08806388225644 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Fixture/appliance dental drill bit, 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Fixture/appliance dental drill bit, reusable

Countersink by Megagen Implant Co. Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fixture/appliance dental drill bit, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 3c7ddbb2-a0a1-406a-83a2-de9320adab58 34 fields · synced May 30, 2026