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MaxMoreSpine

FDA UDI

Class I (US FDA UDI)

by Hoogland Spine Products, GmbH

Identity

Trade Name
MaxMoreSpine FDA UDI
Generic Name
Orthopaedic guidewire, reusable FDA UDI
Device Name
Guide Wires 1.5mm; length 255 mm; FDA UDI
Model / Reference
1001-GW 006 FDA UDI
Description
Guide Wires 1.5mm; length 255 mm; FDA UDI

Identifiers

Primary DI / UDI-DI
04260200313010 FDA UDI
FDA Product Code
HXI FDA UDI
GMDN Term
Orthopaedic guidewire, 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

No

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic guidewire, reusable

MaxMoreSpine by Hoogland Spine Products, GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic guidewire, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 076e9025-e7dd-4d6c-ba82-e77e0ec6717e 33 fields · synced May 31, 2026