Primary Device ID | 10684995520018 |
NIH Device Record Key | 8ea7b21d-a633-467a-a9be-1649242dcc21 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Silicone Tubing, Penrose Drain |
Version Model Number | GR102 |
Company DUNS | 080524654 |
Company Name | BENTEC MEDICAL OPCO, LLC |
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 | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00684995520011 [Primary] |
GS1 | 10684995520018 [Package] Contains: 00684995520011 Package: [25 Units] In Commercial Distribution |
GBX | Catheter, Irrigation |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-10-30 |
Device Publish Date | 2023-10-20 |
10684995520155 | 1 in. x 36 in. Length |
10684995520148 | 3/4 in. x 36 in. Length |
10684995520131 | 1/2 in. x 36 in. Length |
10684995520124 | 1/4 in. x 36 in. Length |
10684995520117 | 1 in. x 18 in. Length |
10684995520100 | 3/4 in. x 18 in. Length |
10684995520094 | 5/8 in. x 18 in. Length |
10684995520087 | 1/2 in. x 18 in. Length |
10684995520070 | 3/8 in. x 18 in. Length |
10684995520063 | 1/4 in. x 18 in. Length |
10684995520056 | 1 in. x 12 in. Length |
10684995520049 | 3/4 in. x 12 in. Length |
10684995520032 | 5/8 in. x 12 in. Length |
10684995520025 | 1/2 in. x 12 in. Length |
10684995520018 | 3/8 in. x 12 in. Length |
10684995520001 | 1/4 in. x 12 in. Length |