Identity
- Trade Name
- NEOSYS FDA UDI
- Generic Name
- Instrument tray, reusable FDA UDI
- Device Name
- NEOSYS CONTAINER S45-S65 328 X 232 X 45 IN2BONES FDA UDI
- Model / Reference
- G01 85011 FDA UDI
- Description
- NEOSYS CONTAINER S45-S65 328 X 232 X 45 IN2BONES FDA UDI
Identifiers
- Catalog Number
- G01 85011 FDA UDI
- Primary DI / UDI-DI
- 03760225714461 FDA UDI
- FDA Product Code
- FSM FDA UDI
- GMDN Term
- Instrument tray, 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
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
MR Conditional FDA UDI
Category: Instrument tray, reusable
Neosys by In2bones — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Instrument tray, reusable.
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- Instrument Case — Katena Products, Inc. · Class I
- Hu-Friedy — Hu-Friedy Manufacturing Co., LLC · Class I
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- ASELTECH — Asel Tibbi Aletler A.S. · Class I
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
- In2bones
Sources (1)
- FDA UDI 3023d10a-97ed-4242-923b-668995f96666 35 fields · synced May 30, 2026