Primary Device ID | 00815212021763 |
NIH Device Record Key | ad34e7e1-9bec-4141-a098-a3be5cea24bf |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Moldcare |
Version Model Number | MC7002 |
Company DUNS | 933506164 |
Company Name | Izi Medical Products, LLC |
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 | 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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00815212021763 [Primary] |
KXH | Cradle, Patient, Radiologic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2017-02-03 |
00815212021800 | MC7006 |
00815212021794 | MC7005 |
00815212021787 | MC7004 |
00815212021770 | MC7003 |
00815212021763 | MC7002 |
00815212021756 | MC7001 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MOLDCARE 75572500 2380500 Live/Registered |
ALCARE CO., LTD. 1998-10-19 |