INT,SlideCath

GUDID 26950900901632

6F, MP, 80cm

Shanghai Kindly Medical Instruments Co., Ltd.

Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use Angiographic catheter, single-use

• Primary Device ID: 26950900901632
• NIH Device Record Key: 0cc72cdf-e2aa-4157-af10-2ec9ba14fdc3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: INT,SlideCath
• Version Model Number: ACMP6F1080
• Company DUNS: 420827639
• Company Name: Shanghai Kindly Medical Instruments Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06950900901638 [Primary]
GS1	26950900901632 [Package]; Contains: 06950900901638; Package: box [5 Units]; In Commercial Distribution
GS1	46950900901636 [Package]; Contains: 06950900901638; Package: carton [60 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K201929

FDA Product Code

• DQO: Catheter, Intravascular, Diagnostic

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-09-19
• Device Publish Date: 2023-09-11

On-Brand Devices [INT,SlideCath]

• 26950900999004: 5F*65cm ,angled
• 26950900998991: 4F*65cm ,angled
• 26950900998984: 5F*100cm ,straight
• 26950900998977: 5F*65cm ,straight
• 26950900998960: 4F*100cm ,straight
• 26950900998953: 4F*65cm, straight
• 26950900973257: 6F, TIG, 100cm
• 26950900973240: 5F, TIG, 100cm
• 26950900972366: 7F, TIG, 100cm
• 26950900969519: 6F,3DRC,100cm
• 26950900960851: 4F, TIG, 100cm
• 26950900957394: 4F VER 100cm
• 26950900952788: 5F, SIMMONS 1, 100cm
• 26950900952672: 6F VER 100cm
• 26950900952658: 5F VER 100cm
• 26950900952641: 5F, BLK, 100cm
• 26950900942253: 7F, TIG1, 100cm
• 26950900942246: 4F, TIG1, 100cm
• 26950900942239: 7F, SON IIIW, 100cm
• 26950900942222: 4F, SON IIIW, 100cm
• 26950900942215: 7F, SON III, 100cm
• 26950900942208: 4F, SON III, 100cm
• 26950900942192: 7F, SON IIW, 100cm
• 26950900942185: 4F, SON IIW, 100cm
• 26950900942178: 7F, SON II, 100cm
• 26950900942161: 4F, SON II, 100cm
• 26950900942154: 7F, SON IW, 100cm
• 26950900942147: 4F, SON IW, 100cm
• 26950900942130: 7F, SON I, 100cm
• 26950900942123: 4F, SON I, 100cm
• 26950900942116: 7F MPB2 100cm
• 26950900942109: 4F MPB2 100cm
• 26950900942093: 7F MPB1 100cm
• 26950900942086: 4F MPB1 100cm
• 26950900942079: 7F MPA2 100cm
• 26950900942062: 4F MPA2 100cm
• 26950900942055: 4F MPA1 100cm
• 26950900942048: 7F IM 100cm
• 26950900942031: 4F IM 100cm
• 26950900942024: 7F, CBR, 100cm
• 26950900942017: 4F, CBR, 100cm
• 26950900942000: 7F, CBL, 100cm
• 26950900941997: 4F, CBL, 100cm
• 26950900941980: 7F, PIG, 110cm
• 26950900941973: 4F, PIG, 100cm, 6 side holes
• 26950900941966: 7F, AR3, 100cm
• 26950900941959: 4F, AR3, 100cm
• 26950900941942: 7F, AR2, 100cm
• 26950900941935: 4F, AR2, 100cm
• 26950900941928: 7F, AR1, 100cm