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Micro Friedman Rongeur

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
MICRO FRIEDMAN RONGEUR FDA UDI
Generic Name
Orthopaedic joint/limb rongeur FDA UDI
Device Name
MICRO FRIEDMAN RONGEUR STRAIGHT TIP RING HANDLE FDA UDI
Model / Reference
1106-076 FDA UDI
Description
MICRO FRIEDMAN RONGEUR STRAIGHT TIP RING HANDLE FDA UDI

Identifiers

Catalog Number
1106-076 FDA UDI
Primary DI / UDI-DI
00192896083332 FDA UDI
FDA Product Code
HTX FDA UDI
GMDN Term
Orthopaedic joint/limb rongeur FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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 — 5.5 Inch FDA UDI

Category: Orthopaedic joint/limb rongeur

Micro Friedman Rongeur by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic joint/limb rongeur.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cbf29756-b586-4b3b-b39b-9dfffe991228 36 fields · synced May 30, 2026