Primary Device ID | 38053326000653 |
NIH Device Record Key | 5958a4c4-e9df-4161-93c9-033b873d0e12 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Inoculation Loops |
Version Model Number | 179CS10 |
Catalog Number | 179CS10 |
Company DUNS | 428981112 |
Company Name | COPAN ITALIA SPA |
Device Count | 50 |
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 | false |
Expiration Date | true |
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 | 18053326000659 [Unit of Use] |
GS1 | 28053326000656 [Primary] |
GS1 | 38053326000653 [Package] Contains: 28053326000656 Package: [4 Units] In Commercial Distribution |
LXG | Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-01-25 |
Device Publish Date | 2024-01-17 |
38053326004323 | HARD LOOP 10 µL STERILE, IN RESEALABLE BAGS OF 40 PCS |
38053326004262 | STERILE HARD 1 µL LOOPS IN RESEALABLE BAG OF 40 PCS |
38053326001186 | SOFT LOOP 10 µL STERILE, IN RESEALABLE BAGS OF 40 PCS |
38053326001179 | SOFT LOOPS 1 UL STERILE, IN BAG OF 20 PCS |
38053326001155 | SOFT LOOPS 1 µL STERILE IN RESEABLE BAG 40 PCS PACKED |
38053326000738 | HARD LOOP 10 µL STERILE, IN BAGS OF 20 PCS |
38053326000721 | HARD LOOP 1 µL STERILE, IN BAGS OF 20 PCS |
38053326000660 | SOFT LOOP 10 µL STERILE, IN BAG OF 20 PCS |
38053326000653 | SOFT LOOP 10 UL STERILE, IN BAG OF 10 PCS |