MaxMoreSpine

FDA UDI

Class I (US FDA UDI)

by Hoogland Spine Products, GmbH

Identity

Trade Name: MaxMoreSpine FDA UDI
Generic Name: Rigid endoscopic scissors, reusable FDA UDI
Device Name: Detachable Hook Scissors Forceps, l = 320 mm, 2.7 mm FDA UDI
Model / Reference: 1001-HS 001-D FDA UDI
Description: Detachable Hook Scissors Forceps, l = 320 mm, 2.7 mm FDA UDI

Identifiers

Primary DI / UDI-DI: 04260200313218 FDA UDI
FDA Product Code: HRR FDA UDI
GMDN Term: Rigid endoscopic scissors, 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

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

Yes

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 endoscopic scissors, reusable

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

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Also classified as Rigid endoscopic scissors, reusable.

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Medicon — Medicon eG. Chirurgiemechaniker-Genossenschaft · Class I
Olympus — Olympus Winter & Ibe GmbH · Class II
ELMED — ELMED INCORPORATED · 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 I	Pending data

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Manufacturer

Manufacturer: Hoogland Spine Products, GmbH

Sources (1)

FDA UDI 8fcfb9eb-9558-4d29-a462-ec57beca07b2 33 fields · synced May 30, 2026