Radpad 7301A-O
by Worldwide Innovations & Technologies, Inc.
Radpad 7301A-O is a Class II device made by Worldwide Innovations & Technologies, Inc., listed in FDA GUDID since 16 Jul 2020 (UDI-DI 00852814003896), registry data as of 22 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 | Number00852814003896 | Date16 Jul 2020 | StatusListed |
Official records
- AccessGUDID record 00852814003896
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Radpad
- Generic name
- Patient radiation shielding pad/drape, single-use
- Model / reference
- 7301A-O
- Primary DI / UDI-DI
- 00852814003896
- FDA product code
- PUI
- GMDN term
- Patient radiation shielding pad/drape, single-use
- Device class
- Class II
- Regulation number
- 878.4370
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
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