Primary Device ID | 06939282458534 |
NIH Device Record Key | 9793cbf2-c6af-44d7-8417-e99eae7dd556 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Linear Stapler |
Version Model Number | FLSL45 4.8 |
Company DUNS | 559966539 |
Company Name | B. J. ZH. F. Panther Medical Equipment Co., Ltd. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06939282458534 [Primary] |
GDW | Staple, Implantable |
Steralize Prior To Use | true |
Device Is Sterile | true |
[06939282458534]
Ethylene Oxide
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-05-07 |
Device Publish Date | 2018-04-04 |
06939282458688 | FLSLF90 4.8 |
06939282458671 | FLSLF90 3.5 |
06939282458664 | FLSLF60 4.8 |
06939282458657 | FLSLF60 3.5 |
06939282458640 | FLSLF45 4.8 |
06939282458633 | FLSLF45 3.5 |
06939282458626 | FLSLF30 4.8 |
06939282458619 | FLSLF30 3.5 |
06939282458602 | FLSLF30 2.5 |
06939282458572 | FLSL90 4.8 |
06939282458565 | FLSL90 3.5 |
06939282458558 | FLSL60 4.8 |
06939282458541 | FLSL60 3.5 |
06939282458534 | FLSL45 4.8 |
06939282458527 | FLSL45 3.5 |
06939282458510 | FLSL30 4.8 |
06939282458503 | FLSL30 3.5 |