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Miot Plating System

FDA UDI

Class II (US FDA UDI)

by Orthofix, Inc.

Identity

Trade Name
MIOT PLATING SYSTEM FDA UDI
Generic Name
Wire cutter FDA UDI
Device Name
MIOT PLATE WIRES CUTTER FDA UDI
Model / Reference
1 FDA UDI
Description
MIOT PLATE WIRES CUTTER FDA UDI

Identifiers

Catalog Number
SP37201 FDA UDI
Primary DI / UDI-DI
18032568868685 FDA UDI
510(k) Number
K051945 FDA UDI
FDA Product Code
HRS FDA UDI
GMDN Term
Wire cutter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Width — 263 Millimeter FDA UDI

Category: Wire cutter

Miot Plating System by Orthofix, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wire cutter.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Orthofix, Inc.

Sources (1)

  • FDA UDI 8ac4a369-9991-4dc1-8a04-2f2e2ad19252 37 fields · synced May 30, 2026