Breathe-EZ MDBB1AY003A
Breathe-EZ MDBB1AY003A is a Class I device made by Micro-tech Usa, listed in FDA GUDID since 3 Mar 2025 (UDI-DI 00850025860031), 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 | Number00850025860031 | Date3 Mar 2025 | StatusListed |
Official records
- AccessGUDID record 00850025860031
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Breathe-EZ
- Generic name
- Endoscopic bite block, basic, single-use
- Model / reference
- MDBB1AY003A
- Primary DI / UDI-DI
- 00850025860031
- FDA product code
- MNK
- GMDN term
- Endoscopic bite block, basic, single-use
- Device class
- Class I
- Regulation number
- 876.1500
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Endoscopic bite block, basic, single-use.
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- Disposable Bite Block VDK-KD-B1 by Jiangsu Vedkang Medical Science and Technology Co., Ltd.
- 00712805 by US Endoscopy
- CONMED 001429 by Conmed Corporation
- Universal Bite Block, Adult 11160 by B&B Medical Technologies, Inc