← Back to catalogue

EasyDrill Cranial Perforator Ø14 x Ø11 x 1, 5mm

FDA UDI

Class II (US FDA UDI)

by Micromar Indústria e Comércio Ltda

Identity

Trade Name
EasyDrill Cranial Perforator Ø14 x Ø11 x 1,5mm FDA UDI
Generic Name
Automatic cranial perforator, single-use FDA UDI
Model / Reference
DM0210FAA FDA UDI

Identifiers

Catalog Number
DM0210FAA FDA UDI
Primary DI / UDI-DI
07898959543357 FDA UDI
510(k) Number
K141455 FDA UDI
FDA Product Code
HBF FDA UDI
GMDN Term
Automatic cranial perforator, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4305 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Automatic cranial perforator, single-use

EasyDrill Cranial Perforator Ø14 x Ø11 x 1, 5mm by Micromar Indústria e Comércio Ltda — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Automatic cranial perforator, single-use.

Cleared under the same submission

K141455 also covers:

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

Manufacturer
Micromar Indústria e Comércio Ltda

Sources (1)

  • FDA UDI a9b12ca8-3fe3-4707-a390-21f6f5c379a9 37 fields · synced May 30, 2026