Primary Device ID | 06970575220117 |
NIH Device Record Key | 5f992147-d501-4adb-88aa-934ccceafa2c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | KD |
Version Model Number | PL001-2004 |
Company DUNS | 544250984 |
Company Name | SUZHOU KD INTELLIGENT DEVICE CO., LTD |
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 | false |
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 | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06970575220117 [Primary] |
ITI | Wheelchair, Powered |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-05-22 |
Device Publish Date | 2024-05-14 |
06970575220179 | PL001-3005 |
06970575220162 | PL001-4001 |
06970575220155 | PL001-7003 |
06970575220148 | PL001-7002 |
06970575220124 | PL001-3003 |
06970575220117 | PL001-2004 |
06970575220100 | PL001-2010 |
06970575220094 | PL001-2003 |
06970575220087 | PL001-8002 |
06970575220186 | PL001-8000 |
06970575220131 | PL001-7000 |
06970575220070 | PL001-6000 |
06970575220063 | PL001-5000 |
06970575220056 | PL001-4000 |
06970575220049 | PL001-3000 |
06970575220032 | PL001-2000 |
06970575220025 | PL001-1000 |
06970575220018 | PL001 |