Primary Device ID | 36945630133559 |
NIH Device Record Key | 2a01116f-3a67-4c4c-9cdd-a45880dcfbca |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FIRST BLADES DISPOSABLE SURGICAL BLADES |
Version Model Number | Standard SS 21# |
Company DUNS | 554434897 |
Company Name | Sterilance Medical (Suzhou) Inc. |
Device Count | 100 |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06945630133558 [Unit of Use] |
GS1 | 16945630133555 [Primary] |
GS1 | 36945630133559 [Package] Contains: 16945630133555 Package: [50 Units] In Commercial Distribution |
GES | Blade, Scalpel |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-01-17 |
Device Publish Date | 2025-01-09 |
36945630133627 | Standard SS 15# |
36945630133610 | Standard SS 10# |
36945630133580 | Standard SS 24# |
36945630133573 | Standard SS 23# |
36945630133566 | Standard SS 22# |
36945630133559 | Standard SS 21# |
36945630133542 | Standard SS 20# |
36945630133535 | Standard SS 15# |
36945630133528 | Standard SS 12# |
36945630133511 | Standard SS 11# |
36945630133504 | Standard SS 10# |
36945630133603 | Standard CS 15# |
36945630133597 | Standard CS 10# |