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Mpfl

FDA UDI

Class I (US FDA UDI)

by Orthopediatrics Corp.

Identity

Trade Name
MPFL FDA UDI
Generic Name
Cannulated surgical drill bit, reusable FDA UDI
Device Name
7MM CANNULATED DRILL, CALIBRATED, TRILOBE DRIVE FDA UDI
Model / Reference
01-1150-0070 FDA UDI
Description
7MM CANNULATED DRILL, CALIBRATED, TRILOBE DRIVE FDA UDI

Identifiers

Catalog Number
01-1150-0070 FDA UDI
Primary DI / UDI-DI
00841132145333 FDA UDI
FDA Product Code
HTW FDA UDI
GMDN Term
Cannulated surgical drill bit, reusable 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

Category: Cannulated surgical drill bit, reusable

Mpfl by Orthopediatrics Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cannulated surgical drill bit, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 91958404-f8d3-4667-8b04-ec205e8894be 35 fields · synced Jun 1, 2026