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Circular Cutting Atrum Punch

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
CIRCULAR CUTTING ATRUM PUNCH FDA UDI
Generic Name
ENT soft-tissue cutting forceps FDA UDI
Device Name
CIRCULAR CUTTING ATRUM PUNCH UP-ANGLE TIP FDA UDI
Model / Reference
468-347 FDA UDI
Description
CIRCULAR CUTTING ATRUM PUNCH UP-ANGLE TIP FDA UDI

Identifiers

Catalog Number
468-347 FDA UDI
Primary DI / UDI-DI
00192896092624 FDA UDI
FDA Product Code
KTF FDA UDI
GMDN Term
ENT soft-tissue cutting forceps 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 — 6.25 Inch FDA UDI

Category: ENT soft-tissue cutting forceps

Circular Cutting Atrum Punch by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as ENT soft-tissue cutting forceps.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e6003770-aa71-43dc-af52-4563583a13d6 36 fields · synced May 30, 2026