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Large Plate/Wire Cutter

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
Large Plate/Wire Cutter FDA UDI
Generic Name
Orthopaedic implantable-device cutter FDA UDI
Device Name
LARGE PLATE/WIRE CUTTER HEAVY DUTY CUTS UP TO 3.5 MILLIMETERS MAXIMUM 9.50 INCHES QUANTUM FDA UDI
Model / Reference
1103-104XQ FDA UDI
Description
LARGE PLATE/WIRE CUTTER HEAVY DUTY CUTS UP TO 3.5 MILLIMETERS MAXIMUM 9.50 INCHES QUANTUM FDA UDI

Identifiers

Primary DI / UDI-DI
00192896106772 FDA UDI
FDA Product Code
HXZ FDA UDI
GMDN Term
Orthopaedic implantable-device cutter 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 — 9.5 Inch FDA UDI

Category: Orthopaedic implantable-device cutter

Large Plate/Wire Cutter by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implantable-device cutter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0afdfaf9-8b27-4ceb-b4a8-86afdf61c9a3 35 fields · synced Jun 6, 2026