Daniels 4500101001
by Daniels Corporation International Pty Ltd
Daniels 4500101001 is a Class I device made by Daniels Corporation International Pty Ltd, listed in FDA GUDID since 11 Feb 2019 (UDI-DI 09333990004378), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number09333990004378 | Date11 Feb 2019 | StatusListed |
Official records
- AccessGUDID record 09333990004378
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Daniels
- Generic name
- Surgical instrument containment holder, single-use, non-sterile
- Model / reference
- 4500101001
- Primary DI / UDI-DI
- 09333990004378
- FDA product code
- FSM
- GMDN term
- Surgical instrument containment holder, single-use, non-sterile
- Device class
- Class I
- Regulation number
- 878.4800
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code FSM (Tray, Surgical, Instrument).
- PST Corp. 4600M by Plastic Sterilizing Tray Corporation
- ACUMED 80-0809 by ACUMED LLC
- APEX Knee System KS-99186 by OMNIlife science, Inc.
- ACUMED 80-2629 by ACUMED LLC
- NA IC 2090-01 by aap Implantate AG
- APEX Knee System KS-90192-IN by OMNIlife science, Inc.
- PST Corp. 1500M by Plastic Sterilizing Tray Corporation
- 5888-00-60 00-5888-000-60 by Zimmer, Inc.
- EVOS Cabling System 56-71175691 by Pioneer Surgical Technology Inc.
- TRACHEOSTOMY CARE TRAY by Medcare Products
Other devices from Daniels Corporation International Pty Ltd
See all devices from Daniels Corporation International Pty Ltd →