Primary Device ID | 08714729298151 |
NIH Device Record Key | 94d934f2-b429-4a32-8863-176936ff61cf |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | M0067402000 |
Catalog Number | M0067402000 |
Company DUNS | 021717889 |
Company Name | BOSTON SCIENTIFIC CORPORATION |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Length | 15 Centimeter |
Length | 15 Centimeter |
Length | 15 Centimeter |
Length | 15 Centimeter |
Length | 15 Centimeter |
Length | 15 Centimeter |
Length | 15 Centimeter |
Length | 15 Centimeter |
Length | 15 Centimeter |
Length | 15 Centimeter |
Length | 15 Centimeter |
Length | 15 Centimeter |
Length | 15 Centimeter |
Length | 15 Centimeter |
Length | 15 Centimeter |
Length | 15 Centimeter |
Length | 15 Centimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08714729298151 [Primary] |
EYK | CONNECTOR, URETERAL CATHETER |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-10-17 |
Device Publish Date | 2024-10-09 |
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00191506043704 - FARASTAR™ | 2024-10-30 Pulsed Field Ablation Generator |
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