Identity
- Trade Name
- MaxMoreSpine FDA UDI
- Generic Name
- Rigid optical arthroscope, reusable FDA UDI
- Device Name
- Endoscopes EUDAMEDTOM Endo Stick 3,7 mm FDA UDI
- Model / Reference
- 1002-TS 001 EUDAMEDFDA UDI
- Description
- TOM Endo Stick 3,7 mm FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04260200311146 EUDAMEDFDA UDI
- Basic UDI-DI
- 426020031MaxmoreTOEnSt4E EUDAMED
- Direct Marketing DI
- 04260200311146 EUDAMED
- FDA Product Code
- HRX FDA UDI
- EMDN Code
- Z12021101 ARTHROSCOPES EUDAMED
- GMDN Term
- Rigid optical arthroscope, reusable FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 888.1100 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Rigid optical arthroscope, reusable
MaxMoreSpine by Hoogland Spine Products, GmbH — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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Also classified as Rigid optical arthroscope, reusable.
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Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class II | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Hoogland Spine Products, GmbH
Sources (2)
- FDA UDI 136e7ec6-3006-4cb0-8064-d4f685eb6b7e 33 fields · synced Aug 1, 2026
- EUDAMED 2ab0828d-0872-45f6-914b-f4d94ddad88f 61 fields · synced Jul 28, 2026