Primary Device ID | 00841494103682 |
NIH Device Record Key | ae7fef9d-d2f2-4af8-8691-d47951b4e37e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LLETZ BAYONET |
Version Model Number | W34 |
Catalog Number | W34 |
Company DUNS | 079095245 |
Company Name | Ellman International |
Device Count | 1 |
DM Exempt | true |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
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 | 00841494103682 [Primary] |
JOS | Electrode, electrosurgical |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-21 |
00841494105242 | LLETZ BAYONET, 5MM BALL STERILE |
00841494105235 | LLETZ BAYONET, 25MM LOOP STERILE |
00841494105228 | LLETZ BAYONET, 20MM LOOP STERILE |
00841494105211 | LLETZ BAYONET, 15MM LOOP STERILE |
00841494103705 | LLETZ BAYONET, 8MM ENDO-CERVICAL, 1/16" |
00841494103682 | LLETZ BAYONET, 5MM BALL 1/16" |
00841494103668 | LLETZ BAYONET, 25MM LOOP 1/16" |
00841494103644 | LLETZ BAYONET, 20MM LOOP 1/16" |
00841494103620 | LLETZ BAYONET, 15MM LOOP 1/16" |