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Gyrus Acmi

FDA UDI

Class I (US FDA UDI)

by Gyrus Acmi, Inc.

Identity

Trade Name
GYRUS ACMI FDA UDI
Generic Name
Diamond ENT bur, single-use FDA UDI
Device Name
MASTOID DIAMOND BURR STERILE 6.0MM DIA X 70MM LENGTH STAINLESS STEEL DISPOSABLE FDA UDI
Model / Reference
70327011 FDA UDI
Description
MASTOID DIAMOND BURR STERILE 6.0MM DIA X 70MM LENGTH STAINLESS STEEL DISPOSABLE FDA UDI

Identifiers

Primary DI / UDI-DI
00821925021204 FDA UDI
FDA Product Code
EQJ FDA UDI
GMDN Term
Diamond ENT bur, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4140 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Diamond ENT bur, single-use

Gyrus Acmi by Gyrus Acmi, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Diamond ENT bur, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gyrus Acmi, Inc.

Sources (1)

  • FDA UDI 852025b6-7040-41b1-8c9f-b0653c5b3bd4 33 fields · synced May 31, 2026