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Micron

FDA UDI

Class II (US FDA UDI)

by Gyrus Acmi, Inc.

Identity

Trade Name
MICRON FDA UDI
Generic Name
Tympanostomy tube FDA UDI
Device Name
MICRON SPOON BOBBIN VENT TUBE 1.27 MM I.D. TITANIUM FDA UDI
Model / Reference
145273-ENT FDA UDI
Description
MICRON SPOON BOBBIN VENT TUBE 1.27 MM I.D. TITANIUM FDA UDI

Identifiers

Primary DI / UDI-DI
00821925039803 FDA UDI
510(k) Number
K820362 FDA UDI
FDA Product Code
ETD FDA UDI
GMDN Term
Tympanostomy tube FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.3880 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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: Tympanostomy tube

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

Similar devices

Also classified as Tympanostomy tube.

Cleared under the same submission

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 4b10ea2f-5957-4db0-9c93-4a123974302f 35 fields · synced May 31, 2026