Primary Device ID | 00684995550049 |
NIH Device Record Key | 3ae97163-d4ec-4d1f-8168-c64ed36ef12b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Silicone Tubing, Bulk |
Version Model Number | BM3-1850 |
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 | 00684995550049 [Primary] |
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 |
00684995550162 | 0.250" ID x 0.375" OD x 50 ft |
00684995550155 | 0.187" ID x 0.375" OD x 50 ft |
00684995550148 | 0.187" ID x 0.312" OD x 50 ft |
00684995550131 | 0.125" ID x 0.250" OD x 50 ft |
00684995550124 | 0.132" ID x 0.183" OD x 50 ft |
00684995550117 | 0.104" ID x 0.192" OD x 50 ft |
00684995550100 | 0.078" ID x 0.125" OD x 50 ft |
00684995550094 | 0.062" ID x 0.188" OD x 50 ft |
00684995550087 | 0.062" ID x 0.125" OD x 50 ft |
00684995550070 | 0.062" ID x 0.095" OD x 50 ft |
00684995550063 | 0.058" ID x 0.077" OD x 50 ft |
00684995550056 | 0.040" ID x 0.085" OD x 50 ft |
00684995550049 | 0.031" ID x 0.156" OD x 50 ft |
00684995550032 | 0.030" ID x 0.065" OD x 50 ft |
00684995550025 | 0.025" ID x 0.047" OD x 50 ft |
00684995550018 | 0.020" ID x 0.037" OD x 50 ft |
00684995550001 | 0.012" ID x 0.025" OD x 50 ft |