AccessGUDID - DEVICE: Reliant(TM) Multistage Dilatation Balloon Catheter (06932503523042)

GUDID

Device Identifier (DI) Information

Brand Name: Reliant(TM) Multistage Dilatation Balloon Catheter
Version or Model: MBD-AS-BB-2
Commercial Distribution Status: In Commercial Distribution
Catalog Number: MBD-AS-BB-2
Company Name: Micro-Tech (Nanjing) Co., Ltd.

Primary DI Number: 06932503523042
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 530269083 *Terms of Use

Device Description: the balloon diameter is 6-7-8mm,the balloon length is 30mm,the catheter diameter is 7 Fr., and the working length is 2300mm,with stainless steel guide wire

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	Yes
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
45712	Gastrointestinal/biliary dilation balloon catheter, non-medicated	A long, thin, flexible tube with an inflatable balloon at its distal tip intended to be used for gastrointestinal and/or biliary intraluminal dilation; it is typically used to endoscopically dilate strictures of the oesophagus, pylorus, colon and/or biliary tract. The balloon is inflated to its prescribed diameter to widen the affected passage of the tract. The device may consist of one or more lumen, may be of the fixed-wire or wire-guided type, and is not coated with a drug/pharmaceutical. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
KNQ	Dilator, Esophageal
FGE	Catheter, Biliary, Diagnostic

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K180418	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
Balloon Length: 30 Millimeter

Device Record Status

Public Device Record Key: 5403c9c6-e72a-4854-be9b-1a0275d017c5
Public Version Date: December 23, 2024
Public Version Number: 5
DI Record Publish Date: March 01, 2016