Primary Device ID | 00853508002072 |
NIH Device Record Key | 2963e77f-6d14-4e93-815b-3d762e364419 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BE-ST ElectroCautery Pencil |
Version Model Number | 1560-02 |
Company DUNS | 958212029 |
Company Name | LACEY MANUFACTURING COMPANY, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Length | 12 Inch |
Length | 12 Inch |
Length | 12 Inch |
Length | 12 Inch |
Length | 12 Inch |
Length | 12 Inch |
Length | 12 Inch |
Length | 12 Inch |
Length | 12 Inch |
Length | 12 Inch |
Length | 12 Inch |
Length | 12 Inch |
Length | 12 Inch |
Length | 12 Inch |
Length | 12 Inch |
Length | 12 Inch |
Length | 12 Inch |
Length | 12 Inch |
Length | 12 Inch |
Length | 12 Inch |
Length | 12 Inch |
Length | 12 Inch |
Length | 12 Inch |
Length | 12 Inch |
Length | 12 Inch |
Length | 12 Inch |
Length | 12 Inch |
Length | 12 Inch |
Length | 12 Inch |
Length | 12 Inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00853508002072 [Primary] |
GEI | Electrosurgical, Cutting & Coagulation & Accessories |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-02-21 |
Device Publish Date | 2016-09-19 |
00853508002140 | Bayonet ElectroCautery Pencil |
00853508002072 | Bayonet ElectroCautery Pencil |