Primary Device ID | 00612649215952 |
NIH Device Record Key | ef806d73-a0be-4404-b719-2b19757855a3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ADULT ULTRA FLEX® |
Version Model Number | 81214F-19121Z |
Catalog Number | 81214F-19121Z |
Company DUNS | 009299017 |
Company Name | King Systems Corporation |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00612649215952 [Package] Contains: 00612649215969 Package: [30 Units] In Commercial Distribution |
GS1 | 00612649215969 [Primary] |
CAI | Circuit, breathing (w connector, adaptor, y piece) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-09-14 |
Device Publish Date | 2022-09-06 |
00612649214696 | ADULT ULTRAFLEX CIRCUIT |
00612649215129 | ADULT ULTRAFLEX CIRCUIT |
00612649141596 | ADULT ULTRAFLEX CIRCUIT |
00612649158754 | ADULT ULTRAFLEX CIRCUIT |
00612649148861 | ADULT ULTRAFLEX CIRCUIT |
00612649172583 | ADULT ULTRAFLEX CIRCUIT |
00612649158723 | ADULT ULTRAFLEX CIRCUIT |
00612649170282 | ADULT ULTRAFLEX CIRCUIT |
00612649135717 | ADULT ULTRAFLEX CIRCUIT |
00612649215631 | ADULT ULTRAFLEX CIRCUIT |
00612649215617 | ADULT ULTRAFLEX CIRCUIT |
00612649215679 | ADULT ULTRA FLEX CIRCUIT PACK KIT |
00612649215587 | ADULT ULTRAFLEX PACK KIT |
00612649215501 | ADULT ULTRAFLEX CIRCUIT |
00612649215938 | ADULT ULTRAFLEX CIRCUIT |
00612649215761 | ADULT ULTRAFLEX CIRCUIT |
00612649215976 | ADULT ULTRAFLEX CIRCUIT |
00612649215952 | ADULT ULTRAFLEX CIRCUIT |
00612649216249 | ADULT ULTRAFLEX CIRCUIT |