Single-Use Ureterorenoscope

Primary DI
06970462546474
Brand
Single-Use Ureterorenoscope
Company
Shenzhen HugeMed Medical Technical Development Co., Ltd.
Model
HU30
Published
2024-06-11
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
FGBUreteroscope And Accessories, Flexible/Rigid

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FGBUreteroscope And Accessories, Flexible/RigidGastroenterology, Urology2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K240374000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K240374000Ureterorenoscope SystemShenzhen HugeMed Medical Technical Development Co., Ltd.2024-05-10FGB

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
16970462546471PackageGS11Not in Commercial Distribution
26970462546478PackageGS110Not in Commercial Distribution
36970462546475PackageGS15Not in Commercial Distribution
06970462546474PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
1697046254647116970462546471
2697046254647826970462546478
3697046254647536970462546475
06970462546474069704625464746970462546474

GMDN Terms#

Term, Definition table
TermDefinition
Flexible video ureterorenoscope, single-useAn endoscope with a flexible inserted portion intended for the visual examination and treatment of the ureter and renal pelvis. It is inserted through the external urethral orifice or a surgically-created percutaneous route during a urological procedure. Anatomical images are transmitted to the user by a video system with an electronic image sensor at the distal end of the endoscope and the images showing on a monitor. This device is commonly used for the removal or crushing of stones, and evaluation of pyelitis and renal failure. This is a single-use device.

Regulatory Flags#

DUNS number
403655303
Device count
1
Serial number
true
Manufacturing date on label
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
06970462546719Broncho SamplerBS012026-02-10
06970462546856Stone Collector180ML-L2026-02-10
06970462547457Single-use Ureteral Access SheathY-08-362026-02-10
06970462547464Single-use Ureteral Access SheathY-08-402026-02-10
06970462547471Single-use Ureteral Access SheathY-08-452026-02-10
06970462547488Single-use Ureteral Access SheathY-08-502026-02-10
06970462547495Single-use Ureteral Access SheathY-08-552026-02-10
06970462547501Single-use Ureteral Access SheathY-09-362026-02-10
06970462547518Single-use Ureteral Access SheathY-09-452026-02-10
06970462547525Single-use Ureteral Access SheathY-09-552026-02-10
06970462547532Single-use Ureteral Access SheathY-10-362026-02-10
06970462547549Single-use Ureteral Access SheathY-10-452026-02-10
06970462547556Single-use Ureteral Access SheathY-10-552026-02-10
06970462547563Single-use Ureteral Access SheathY-11-362026-02-10
06970462547570Single-use Ureteral Access SheathY-11-452026-02-10
06970462547587Single-use Ureteral Access SheathY-11-552026-02-10
06970462547594Single-use Ureteral Access SheathY-12-362026-02-10
06970462547600Single-use Ureteral Access SheathY-12-452026-02-10
06970462547617Single-use Ureteral Access SheathY-12-552026-02-10
16970462546716Broncho SamplerBS012026-02-10

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Primary DI, Brand, Company table
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16972304750428DeepEyeSurgnova Healthcare Technologies (Zhejiang) Co., Ltd.FGB2026-05-22
16972304750435DeepEyeSurgnova Healthcare Technologies (Zhejiang) Co., Ltd.FGB2026-05-22
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00810116024094Dornier MedTech DORNIER MEDTECH AMERICA, INC.FGB2026-03-26
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