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Diego

FDA UDI

Class II (US FDA UDI)

by Gyrus Acmi, Inc.

Identity

Trade Name
Diego FDA UDI
Generic Name
ENT shaver system FDA UDI
Device Name
DIEGO UNIVERSAL IGS ADAPTER LARGE STAINLESS STEEL FDA UDI
Model / Reference
70338013 FDA UDI
Description
DIEGO UNIVERSAL IGS ADAPTER LARGE STAINLESS STEEL FDA UDI

Identifiers

Primary DI / UDI-DI
00821925026186 FDA UDI
510(k) Number
K030343 FDA UDI
FDA Product Code
HAW FDA UDI
GMDN Term
ENT shaver system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4560 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

No

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: ENT shaver system

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

Similar devices

Also classified as ENT shaver system.

Cleared under the same submission

K030343 also covers:

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 6317581c-cc66-4970-8833-3bd1fdcd0a37 34 fields · synced Jun 1, 2026