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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
Rigid endoscopic biopsy forceps, reusable FDA UDI
Device Name
Rotational Punch shaft 2.0mm FDA UDI
Model / Reference
1001-EP 006 FDA UDI
Description
Rotational Punch shaft 2.0mm FDA UDI

Identifiers

Primary DI / UDI-DI
04260200313485 FDA UDI
FDA Product Code
LRY 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

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

Similar devices

Also classified as Rigid endoscopic biopsy forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cc157a19-d8d9-4d87-a5c7-9e109ac7372b 33 fields · synced May 30, 2026