Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3031983053

FEI Number

3031983053

Entity Name

DAMBO SRL

City/State/Country

Putignano Bari, IT

Establishment Address

Via Maestri Del Lavoro, Putignano Bari 70017, IT

Establishment Type(s)

Repack or Relabel Medical Device,Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

Dambo SRL (Owner Number: 10091247)

Owner / Operator Contact Address

Via Maestri Del Lavoro, Putignano, IT-BA 70017, IT

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

P170007

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MOZ	Acid, Hyaluronic, Intraarticular	Unknown	Class 3	N/A	2025-09-16
MOZ	Acid, Hyaluronic, Intraarticular	Unknown	Class 3	N/A	2024-09-29
FMF	Syringe, Piston	General Hospital	Class 2	880.5860	2025-04-18
MOZ	Acid, Hyaluronic, Intraarticular	Unknown	Class 3	N/A	2025-11-24
FOZ	Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days	General Hospital	Class 2	880.5200	2024-07-31
DYB	Introducer, Catheter	Cardiovascular	Class 2	870.1340	2024-07-31
MOZ	Acid, Hyaluronic, Intraarticular	Unknown	Class 3	N/A	2025-09-17

Official Correspondent

Simone Mancazzo

US Agent Details

FDAIMPORTS.COM LLC Email: registration@fdaimports.com Phone: (410) 2202800

Related Public Records

Same Entity

Dambo SRL

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
K880350	Honway International Co.	YUE/FA DISPOSABLE SYRINGE	1988-02-16
K003571	Terumo Medical Corp.	SERONO FOR USE WITH GONAL-F 1200IU MULTI-DOSE ONLY AT 600IU/ML SYRINGE	2001-02-12
K943349	Quinton, Inc.	MAHURKAR DUAL LUMEN CATHETER	1995-03-22
K912158	Medical Device Inspection Co., Inc.	CENTRAL VENOUS CATHETER DRESSING CHANGE TRAY	1991-10-23
K101883	St Jude Medical	6F ENGAGE/ENGAGE TR INTRODUCER	2010-09-07

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0003-04	Liberty Medical Supplies	2	Liberty brand Insulin Syringes for use with U-100 insulin, 1/2 cc X 30G X 5/16'' syringes
Z-0004-04	Liberty Medical Supplies	2	Liberty brand Insulin Syringes for use with U-100 insulin, 1 cc X 29G X 1/2 '' insulin syringes
Z-0005-04	Liberty Medical Supplies	2	Liberty brand Insulin Syringes for use with U-100 insulin, 1/2 cc X 29G X 1/2 '' insulin syringes
Z-0005-2024	Fresenius Medical Care Holdings, Inc.	2	10ML SYRINGE LUER LOCK W/OUT NEEDLE, Part Number 15-R010-0, 100 per box, 12 boxes to a case
Z-0006-2024	Fresenius Medical Care Holdings, Inc.	2	10ML SYRINGE LUER LOCK W/NEEDLE, Part Number 15-10ML-0, 100 per box, 12 boxes per case

Similar Registrations

Registration Number	Establishment Name	Location
3043045982	BEAUTYXPORT S.R.O.	Zizkov Praha, Hlavni Mesto, CZ
3033486016	SAIMA GLOBAL FARMA S.L.	GIRONA Gerona, ES
3043624366	10122110 MANITOBA LTD. O/A FORT GARRY MEDICAL SUPPLIES	Winnipeg Manitoba, CA
3003184440	Meiji Pharma Spain	Alcala de Henares Madrid (Province), ES
3015373820	ARCERA GMBH	Munich Bavaria, DE

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3031983053. Last updated year: 2026. Please use registration number 3031983053 when referencing this establishment in official correspondence.