Clinical Guard CMS 50DL
Clinical Guard CMS 50DL is a Class II device made by Clinical Guard, listed in FDA GUDID since 8 Jun 2017 (UDI-DI 00897429002520), 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 | Number00897429002520 | Date8 Jun 2017 | StatusListed |
Official records
- AccessGUDID record 00897429002520
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Clinical Guard
- Generic name
- Pulse oximeter
- Model / reference
- CMS 50DL
- Primary DI / UDI-DI
- 00897429002520
- FDA product code
- OCH
- GMDN term
- Pulse oximeter
- Device class
- Class II
- Regulation number
- 870.2700
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
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- MIR Spirobank Oxi by MIR MEDICAL INTERNATIONAL RESEARCH SPA
- CONTEC CMS50DL1 by Contec Medical Systems Co., Ltd.
- RAD-G 9895 by MASIMO CORPORATION
- Viatom PO6 Oxyfit Pulse Oximeter by Viatom Technology Co., Ltd.
- iHealth PO3M by Ihealth Labs, Inc.