Identity
- Trade Name
- Neoss Implant System FDA UDI
- Generic Name
- Instrument tray, reusable FDA UDI
- Device Name
- Tack Cassette FDA UDI
- Model / Reference
- 64032 FDA UDI
- Description
- Tack Cassette FDA UDI
Identifiers
- Catalog Number
- 64032 FDA UDI
- Primary DI / UDI-DI
- 05060440332845 FDA UDI
- FDA Product Code
- NDP FDA UDI
- GMDN Term
- Instrument tray, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.3980 FDA UDI
- Commercial Distribution
- Not 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
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
No
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
Neoss Implant System by Neoss, Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Neoss, Ltd.
Sources (1)
- FDA UDI f6df6dbd-022b-4abc-9d87-e963c35ce832 36 fields · synced May 30, 2026