Primary Device ID | 10816765014292 |
NIH Device Record Key | 8d8ed056-bb02-4d4d-89a1-a8bcb1e6d4ef |
Commercial Distribution Discontinuation | 2020-03-31 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Histoguide wire guided forceps |
Version Model Number | 00711660 |
Catalog Number | 00711660 |
Company DUNS | 627879687 |
Company Name | US Endoscopy |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx | |
Phone | +1(800)548-4873 |
xx@xx.xx |
Length | 2300 Millimeter |
Length | 2300 Millimeter |
Length | 2300 Millimeter |
Length | 2300 Millimeter |
Length | 2300 Millimeter |
Length | 2300 Millimeter |
Handling Environment Temperature | Between 15 Degrees Celsius and 25 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00816765014295 [Primary] |
GS1 | 10816765014292 [Package] Contains: 00816765014295 Package: Box [5 Units] Discontinued: 2020-03-31 Not in Commercial Distribution |
PTS | Endoscopic grasping/cutting instrument, non-powered, exempt |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-03-31 |
Device Publish Date | 2018-07-30 |
10816765014292 | The Histoguide wire guided forceps are disposable flexible wire-guided forceps used to sample ti |
10724995184060 | The Histoguide wire guided forceps are disposable flexible wire-guided forceps used to sample ti |