ProGear RP88020
ProGear RP88020 is a Class II device made by Prestige Ameritech, listed in FDA GUDID since 26 Sep 2016 (UDI-DI 00852212003320), 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 | Number00852212003320 | Date26 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 00852212003320
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- ProGear
- Generic name
- Surgical/medical face mask, single-use
- Model / reference
- RP88020
- Primary DI / UDI-DI
- 00852212003320
- FDA product code
- FXX
- GMDN term
- Surgical/medical face mask, single-use
- Device class
- Class II
- Regulation number
- 878.4040
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code FXX (Mask, Surgical).
- Aurelia Surgical Mask ASTM Level 1; Aurelia Surgical Mask ASTM Level 2 by Supermax Healthcare Canada-Supermax Medical
- Anti-for Surgical Face Mask by Anago, Inc.
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- Fluidshield Surgical Masks by Tecnol New Jersey Wound Care, Inc.
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- PMW01 Procedure Mask Level 1 by Defender Safety, Inc.
- Protectaide Biohazard Clean-Up Kit No. B3069 by Protectaide, Inc.
- BASE4 Disposable Medical Mask by Base4 Group, Inc.
- Non-Sterile Surgical Mask by A.R. Medicom, Inc.