Identity
- Trade Name
- MaxMoreSpine FDA UDI
- Generic Name
- Bone curette, reusable FDA UDI
- Device Name
- Endoscopes EUDAMEDAbrasions device spoon tip, bent FDA UDI
- Model / Reference
- 1002-TS 008 EUDAMED1001-ABR 4 FDA UDI
- Description
- Abrasions device spoon tip, bent FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04260200310040 EUDAMEDFDA UDI
- Basic UDI-DI
- 426020031MaxmoreTOEnSt4E EUDAMED
- Direct Marketing DI
- 04260200310040 EUDAMED
- FDA Product Code
- FZS FDA UDI
- EMDN Code
- Z12021101 ARTHROSCOPES EUDAMED
- GMDN Term
- Bone curette, reusable FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass I FDA UDI
- Regulation Number
- 878.4800 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Bone curette, reusable
MaxMoreSpine by Hoogland Spine Products, GmbH — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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Also classified as Bone curette, reusable.
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- Medicon — Medicon eG. Chirurgiemechaniker-Genossenschaft · Class I
- Volkmann Bone Curette Oval - Fig. 00 17 cm - 6 3/4" Scoop Size 4.4 mm Stainless Steel — SURTEX INSTRUMENTS LTD · Class I
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 I | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Hoogland Spine Products, GmbH
Sources (2)
- FDA UDI 24e31d92-c91d-4920-a709-c773100600f3 33 fields · synced Jun 18, 2026
- EUDAMED 9215ff79-be9f-4e36-8b66-aacc452b9d0e 61 fields · synced Jun 18, 2026