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Bruns Curette

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
Bruns Curette FDA UDI
Generic Name
Bone curette, reusable FDA UDI
Device Name
Bruns Curette Hexagonal Handle Oval Cup Angle Size 2 FDA UDI
Model / Reference
320-874A FDA UDI
Description
Bruns Curette Hexagonal Handle Oval Cup Angle Size 2 FDA UDI

Identifiers

Primary DI / UDI-DI
00192896106475 FDA UDI
FDA Product Code
HTF FDA UDI
GMDN Term
Bone 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

Dimensions & Sizes

Size
Length — 9 Inch FDA UDI

Category: Bone curette, reusable

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

Similar devices

Also classified as Bone curette, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0736f19c-1ce7-44e7-8d9a-7be3880359f4 35 fields · synced May 31, 2026