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Bayonet Ring Curette

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
BAYONET RING CURETTE FDA UDI
Generic Name
Neurosurgical curette, reusable FDA UDI
Device Name
BAYONET RING CURETTE DOWN ANGLE SHAFT TITANIUM FDA UDI
Model / Reference
413-063 FDA UDI
Description
BAYONET RING CURETTE DOWN ANGLE SHAFT TITANIUM FDA UDI

Identifiers

Catalog Number
413-063 FDA UDI
Primary DI / UDI-DI
00192896036802 FDA UDI
FDA Product Code
HTF FDA UDI
GMDN Term
Neurosurgical curette, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Category: Neurosurgical curette, reusable

Bayonet Ring Curette by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Neurosurgical curette, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sontec Instruments, Inc.

Sources (1)

  • FDA UDI d93e8c3f-4978-4544-b899-a9b44196d7b8 36 fields · synced May 30, 2026