MaxMoreSpine

FDA UDI

Class I (US FDA UDI)

by Hoogland Spine Products, GmbH

Identity

Trade Name: MaxMoreSpine FDA UDI
Generic Name: Rigid endoscopic biopsy forceps, reusable FDA UDI
Device Name: Detachable MaxDisc Grasping forceps 250 mm / Ø 4.0 mm FDA UDI
Model / Reference: 1001-MF 002-D FDA UDI
Description: Detachable MaxDisc Grasping forceps 250 mm / Ø 4.0 mm FDA UDI

Identifiers

Primary DI / UDI-DI: 04260200314055 FDA UDI
FDA Product Code: HTD FDA UDI
GMDN Term: Rigid endoscopic biopsy forceps, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 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 biopsy forceps, reusable

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

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Hermann Medizintechnik GmbH — Hermann Medizintechnik GmbH · Class II
RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · Class I
ELMED — ELMED INCORPORATED · Class II
UTERINE BIOSPY TRIANGULAR BASKET PUNCH — SONTEC INSTRUMENTS, INC. · Class I
Biopsy forceps — Suzhou AcuVu Medical Technology Co., Ltd. · Class I

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 6b53beb3-0297-412d-a7b7-d26d3d6e430e 33 fields · synced May 30, 2026