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Neoss Implant System
FDA UDIEUDAMEDClass I (US FDA UDI)
Ref 51187
by Neoss, Ltd.
Identity
- Trade Name
- Neoss Surgical and Prosthetic Tray - ProActive® Straight EUDAMEDNeoss Implant System FDA UDI
- Generic Name
- Instrument tray, reusable FDA UDI
- Device Name
- Storage EUDAMEDNeoss Surgical and Prosthetic Tray – ProActive® Straight FDA UDI
- Model / Reference
- 51187 EUDAMEDFDA UDI
- Description
- Neoss Surgical and Prosthetic Tray – ProActive® Straight FDA UDI
Identifiers
- Catalog Number
- 51187 FDA UDI
- Primary DI / UDI-DI
- 05060440335709 EUDAMEDFDA UDI
- Basic UDI-DI
- 506044033N0028N7 EUDAMED
- Direct Marketing DI
- 05060440335709 EUDAMED
- FDA Product Code
- NDP FDA UDI
- EMDN Code
- P01020180 DENTAL IMPLANTS - ACCESSORIES EUDAMED
- GMDN Term
- Instrument tray, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 872.3980 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
No
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
Yes
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: Instrument tray, reusable
Neoss Implant System by Neoss, Ltd. — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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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 I | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Neoss, Ltd.
Sources (2)
- FDA UDI 057c2732-70a8-4444-8434-2b96cdf12f91 35 fields · synced Jun 19, 2026
- EUDAMED 5b60b8b3-9a9f-4d7d-8fbc-39bd9c1cdcc1 61 fields · synced Jun 19, 2026