RESTEC SOLUTIONS, LLC

FDA Registration(s)#

Registration, FEI, Name table
Registration	FEI	Name	Status	Initial importer	Expiration year	Address
3043861826	3043861826	RESTEC SOLUTIONS, LLC	1	N	2026-01-01	6350 Quadrangle Dr Ste 140 Chapel Hill NC US 27517

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDID	Product	Phone	Email
00860009496903	SONOPRO - SONOPRO is a limited pre-production run of Automated Disinfector Devices. It is classified by the FDA as a Class II medical device, product code MEC. It is intended for use in the critical care areas of the hospital clinical setting, disinfecting Spaulding category low-risk hand-held re-useable medical devices. Devices must be first pre-cleaned or free of visible bioburden.	7722421900	pbaumgartner@restecs.com

restecs.com

Registered Device Listings#

Registration key, Listing key table
Registration key	Listing key
349172	1773142528

GUDID#

SONOPRO - SONOPRO is a limited pre-production run of Automated Disinfector Devices. It is classified by the FDA as a Class II medical device, product code MEC. It is intended for use in the critical care areas of the hospital clinical setting, disinfecting Spaulding category low-risk hand-held re-useable medical devices. Devices must be first pre-cleaned or free of visible bioburden.

Restec Solutions LLC

2023-03-31