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Arthroscopic Ring Curette

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
ARTHROSCOPIC RING CURETTE FDA UDI
Generic Name
Bone curette, reusable FDA UDI
Device Name
ARTHROSCOPIC RING CURETTE ANGLED SHARP RING TIP TRIANGLE HANDLE FDA UDI
Model / Reference
1271-149 FDA UDI
Description
ARTHROSCOPIC RING CURETTE ANGLED SHARP RING TIP TRIANGLE HANDLE FDA UDI

Identifiers

Catalog Number
1271-149 FDA UDI
Primary DI / UDI-DI
00192896057135 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 — 9.25 Inch FDA UDI

Category: Bone curette, reusable

Arthroscopic Ring 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 ab6412dd-748b-49c8-8dc8-77e8782afe01 36 fields · synced May 31, 2026