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Evonos

FDA UDI

Class II (US FDA UDI)

by Evonos GmbH & Co. KG

Identity

Trade Name
Evonos FDA UDI
Generic Name
Automatic cranial perforator, single-use FDA UDI
Device Name
evoDrill Cranial Perforator, Ø14/11mm, ab 1mm, 3 Flute FDA UDI
Model / Reference
26-000008 FDA UDI
Description
evoDrill Cranial Perforator, Ø14/11mm, ab 1mm, 3 Flute FDA UDI

Identifiers

Primary DI / UDI-DI
04054462020959 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Automatic cranial perforator, single-use

Evonos by Evonos GmbH & Co. KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Automatic cranial perforator, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 46a54b83-da23-4741-90e5-d7c2c0f933d3 33 fields · synced May 30, 2026