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Sontec Ear Raspatory

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
SONTEC EAR RASPATORY FDA UDI
Generic Name
Middle ear file/rasp FDA UDI
Device Name
SONTEC EAR RASPATORY SERRATED CURVED LEFT SHAFT FDA UDI
Model / Reference
475-600 FDA UDI
Description
SONTEC EAR RASPATORY SERRATED CURVED LEFT SHAFT FDA UDI

Identifiers

Catalog Number
475-600 FDA UDI
Primary DI / UDI-DI
00192896042537 FDA UDI
FDA Product Code
JYY FDA UDI
GMDN Term
Middle ear file/rasp FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 7.25 Inch FDA UDI

Category: Middle ear file/rasp

Sontec Ear Raspatory by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Middle ear file/rasp.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e8e845a7-a175-4aa7-8a22-2f50224f9300 36 fields · synced May 31, 2026