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Ballenger Swivel Knife

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
BALLENGER SWIVEL KNIFE FDA UDI
Generic Name
Nasal knife FDA UDI
Device Name
BALLENGER SWIVEL KNIFE BAYONET SWIVEL END FDA UDI
Model / Reference
467-5314 FDA UDI
Description
BALLENGER SWIVEL KNIFE BAYONET SWIVEL END FDA UDI

Identifiers

Catalog Number
467-5314 FDA UDI
Primary DI / UDI-DI
00192896040274 FDA UDI
FDA Product Code
KAS FDA UDI
GMDN Term
Nasal knife 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 — 8.75 Inch FDA UDI

Category: Nasal knife

Ballenger Swivel Knife by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasal knife.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bac40d2b-443f-4e48-b111-4eec4cc3920a 36 fields · synced May 30, 2026