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Skeeter®

FDA UDI

Class II (US FDA UDI)

by Medtronic Xomed, Inc.

Identity

Trade Name
Skeeter® FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
TRAY 3155615 OTO-TOOL STERILIZATION FDA UDI
Model / Reference
3155615 FDA UDI
Description
TRAY 3155615 OTO-TOOL STERILIZATION FDA UDI

Identifiers

Primary DI / UDI-DI
00763000172145 FDA UDI
510(k) Number
K081475 FDA UDI
FDA Product Code
HRX FDA UDI
ERL FDA UDI
HBE FDA UDI
HWE FDA UDI
HBC FDA UDI
GMDN Term
Instrument tray, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.1100 FDA UDI
874.4250 FDA UDI
882.4310 FDA UDI
878.4820 FDA UDI
882.4360 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Instrument tray, reusable

Skeeter® by Medtronic Xomed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument tray, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 24e9d12a-b5d5-45b6-ba29-6517d4fee88b 35 fields · synced May 30, 2026