← Back to catalogue

Medtronic Reusable Instruments

FDA UDI

Class I (US FDA UDI)

by Medtronic Sofamor Danek, Inc.

Identity

Trade Name
Medtronic Reusable Instruments FDA UDI
Generic Name
Surgical flat-nosed pliers FDA UDI
Device Name
BENDING IRON EX1017026 STRAIGHT RIGHT FDA UDI
Model / Reference
EX1017026 FDA UDI
Description
BENDING IRON EX1017026 STRAIGHT RIGHT FDA UDI

Identifiers

Primary DI / UDI-DI
00763000076405 FDA UDI
FDA Product Code
HXW FDA UDI
GMDN Term
Surgical flat-nosed pliers 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical flat-nosed pliers

Medtronic Reusable Instruments by Medtronic Sofamor Danek, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical flat-nosed pliers.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 7d0c7d32-1ee0-4059-a09d-b38d9bdc9d66 34 fields · synced May 30, 2026