Primary Device ID | 00844505005937 |
NIH Device Record Key | d8b24147-e775-4d6e-838b-49ebdd2feaab |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ECLIPSE DE LA CRUZ PISTON |
Version Model Number | 469-400 |
Company DUNS | 030849173 |
Company Name | Grace Medical, Inc. |
Device Count | 1 |
DM Exempt | true |
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 | 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 |
Phone | +1(866)472-2363 |
info@gracemedical.com | |
Phone | +1(866)472-2363 |
info@gracemedical.com | |
Phone | +1(866)472-2363 |
info@gracemedical.com | |
Phone | +1(866)472-2363 |
info@gracemedical.com |
Storage Environment Temperature | Between 0 and 140 Degrees Fahrenheit |
Storage Environment Temperature | Between 0 and 140 Degrees Fahrenheit |
Storage Environment Temperature | Between 0 and 140 Degrees Fahrenheit |
Storage Environment Temperature | Between 0 and 140 Degrees Fahrenheit |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00844505005937 [Primary] |
ETB | PROSTHESIS, PARTIAL OSSICULAR REPLACEMENT |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-02-18 |
00844505005968 | ECLIPSE PISTON DE LA CRUZ 0.6MM DIA X 4.75MM L NITINOL/FLUOROPLASTIC |
00844505005951 | ECLIPSE PISTON DE LA CRUZ 0.6MM DIA X 4.50MM L NITINOL/FLUOROPLASTIC |
00844505005944 | ECLIPSE PISTON DE LA CRUZ 0.6MM DIA X 4.25MM L NITINOL/FLUOROPLASTIC |
00844505005937 | ECLIPSE PISTON DE LA CRUZ 0.6MM DIA X 4.00MM L NITINOL/FLUOROPLASTIC |