MaxMoreSpine

FDA UDI

Class II (US FDA UDI)

by Hoogland Spine Products, GmbH

Identity

Trade Name: MaxMoreSpine FDA UDI
Generic Name: Rigid optical arthroscope, reusable FDA UDI
Device Name: TOM Endo Stick FDA UDI
Model / Reference: 1002-TS 007 FDA UDI
Description: TOM Endo Stick FDA UDI

Identifiers

Primary DI / UDI-DI: 04260200314079 FDA UDI
FDA Product Code: HRX FDA UDI
GMDN Term: Rigid optical arthroscope, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.1100 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Rigid optical arthroscope, reusable

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

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HOPKINS — Karl Storz GmbH & Co. KG · Class II
Olympus — Olympus Winter & Ibe GmbH · Class II
Surgical Direct — SURGICAL DIRECT, INC. · Class II
HOPKINS — Karl Storz GmbH & Co. KG · Class II
Precision Ideal Eyes — Stryker Corp. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Hoogland Spine Products, GmbH

Sources (1)

FDA UDI bec6c805-38b4-44f8-b404-023704e97e38 33 fields · synced May 31, 2026