Multix Solutions SRL X1
by Multix Solutions SRL 2 variants
Multix Solutions SRL X1 (SC_2.101213) is a Class I device made by Multix Solutions SRL, listed in FDA GUDID since 24 Sep 2021 (UDI-DI G035SC21012130), 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 | NumberG035SC21012130 | Date24 Sep 2021 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Multix Solutions SRL
- Generic name
- Electromechanical device/system transport trolley
- Model / Ref / Catalog
- X1, SC_2.101213
- Primary DI / UDI-DI
- G035SC21012130
- FDA product code
- BZN
- GMDN term
- Electromechanical device/system transport trolley
- Device class
- Class I
- Regulation number
- 868.6175
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
Similar devices in this category
Other devices filed under Electromechanical device/system transport trolley.
- Trolley for Basic and Dominant Flex 071.0034 by Medela AG
- BladderScan® Prime 0800-0532 by VERATHON INC
- seca 402 4020000009 by seca GmbH & Co. KG
- Arthrex® ABS-10100 by Arthrex, Inc.
- BladderScan® i10™ 0800-0631 by VERATHON INC
- Megadyne 1300SJ by Megadyne Medical Products, Inc.
- CONMED AS-ICART-V by Conmed Corporation
- DUALTO Energy System ETHCRT by Ethicon Endo-Surgery, LLC
- Emprint CART1 by Covidien LP