Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

9680909

FEI Number

3004150667

Entity Name

C.B.M. S.R.L. a socio unico

City/State/Country

TORRE DE PICENARDI Cremona, IT

Establishment Address

VIA CASTELLO 10/A, TORRE DE PICENARDI Cremona 26038, IT

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

C.B.M. S.R.L. (Owner Number: 9012260)

Owner / Operator Contact Address

VIA CASTELLO 10/A, --, TORRE DE'PICENARDI, CR, IT-NOTA 26038, IT

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

BEDPAN TRAY FOR INSTRUMENTS URINAL KIDNEY DISH

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FSM	Tray, Surgical, Instrument	General, Plastic Surgery	Class 1	878.4800	2007-10-16
FOB	Bedpan	General Hospital	Class 1	880.6730	2007-10-16
LRP	Tray, Surgical	General, Plastic Surgery	Class 1	878.4800	2007-10-16
FNP	Urinal	General Hospital	Class 1	880.6730	2007-10-16
FNY	Basin, Emesis	General Hospital	Class 1	880.6730	2007-10-16

Official Correspondent

CARLO BUSATTI

US Agent Details

ANGELIKA SCHERP Business: BUSINESS SUPPORT INTERNATIONAL Email: info@bsi-fda.com Phone: (212) 3318358

Related Public Records

Same Entity

C.B.M. S.R.L.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K881095	CooperVision, Inc.	KOI(TM) INSTRUMENT TRAYS	1988-04-06

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0027-2016	Zimmer, Inc.	1	Zimmer Universal Locking System, Titanium 3.5mm. Zimmer Implant and Instrument Cases are reusable, non-implantable devices designed to facilitate organization, identification, storage, transportation, cleaning, and sterilization processing of reusable instruments and certain unused implantable devices.
Z-0036-2010	Alphatec Spine, Inc.	1	ROC Lumbar bolt caddy, Part Number: 81997-01-05. Sterilization container for ROC bolts/screws. Product is used to contain spinal implants.

Similar Registrations

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3008886285	Flextronics International Kft	Budapest, HU
3012574325	HAKAMA AG	Baettwil Solothurn, CH
3001397320	ROECHLING MEDICAL ROCHESTER L.P.	Rochester, NY, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9680909. Last updated year: 2026. Please use registration number 9680909 when referencing this establishment in official correspondence.