Tipless Basket TIPL1300

GUDID 03700512978213

1.3 Fr Basket

Promepla

Biliary/urinary stone retrieval basket, single-use Biliary/urinary stone retrieval basket, single-use Biliary/urinary stone retrieval basket, single-use Biliary/urinary stone retrieval basket, single-use Biliary/urinary stone retrieval basket, single-use Biliary/urinary stone retrieval basket, single-use Biliary/urinary stone retrieval basket, single-use Biliary/urinary stone retrieval basket, single-use Biliary/urinary stone retrieval basket, single-use Biliary/urinary stone retrieval basket, single-use Biliary/urinary stone retrieval basket, single-use Biliary/urinary stone retrieval basket, single-use Biliary/urinary stone retrieval basket, single-use Biliary/urinary stone retrieval basket, single-use

• Primary Device ID: 03700512978213
• NIH Device Record Key: a0be3368-23ad-481e-97ec-9bc3dd7f4648
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Tipless Basket
• Version Model Number: ROSZ1300ST245
• Catalog Number: TIPL1300
• Company DUNS: 401020409
• Company Name: Promepla
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	03700512968214 [Primary]
GS1	03700512978213 [Package]; Contains: 03700512968214; Package: Box 1 [1 Units]; In Commercial Distribution
GS1	03700512988212 [Package]; Package: Box 2 [4 Units]; In Commercial Distribution

FDA Product Code

• FFL: Dislodger, Stone, Basket, Ureteral, Metal

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: 2021-03-04
• Device Publish Date: 2021-02-24

Devices Manufactured by Promepla

• 03700512921967 - Y-CLIC ADAPTER: 2024-01-15
• 03700512987451 - LumaFlex Double J stent, 2 open tips, Ch/Fr4,8/L.22cm, without wire: 2024-01-15
• 03700512987468 - LumaFlex Double J stent, 2 open tips, Ch/Fr4,8/L.24cm, without wire: 2024-01-15
• 03700512987475 - LumaFlex Double J stent, 2 open tips, Ch/Fr4,8/L.26cm, without wire: 2024-01-15
• 03700512987482 - LumaFlex Double J stent, 2 open tips, Ch/Fr4,8/L.28cm, without wire: 2024-01-15
• 03700512987499 - LumaFlex Double J stent, 2 open tips, Ch/Fr4,8/L.30cm, without wire: 2024-01-15
• 03700512987505 - LumaFlex Double J stent, 2 open tips, Ch/Fr6/L.24cm, without wire: 2024-01-15
• 03700512977513 - LumaFlex Double J stent, 2 open tips, Ch/Fr6/L.26cm, without wire: 2024-01-15