Primary Device ID | 00845275005127 |
NIH Device Record Key | 61faf272-5245-4d9a-aff8-c314e322dc4b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Thermo Scientific Protocol™ Parasitology System |
Version Model Number | 23-005-51 |
Company DUNS | 183998769 |
Company Name | Fisher Diagnostics |
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 | false |
OTC Over-The-Counter | false |
Phone | 800-528-0494 |
xx@xx.xx |
Storage Environment Temperature | Between 15 Degrees Celsius and 30 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00845275005127 [Primary] |
GS1 | 00845275006490 [Unit of Use] |
LIO | Device, Specimen Collection |
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 | 2016-09-16 |
00845275005134 | 23-005-68 |
00845275005127 | 23-005-51 |
00845275005110 | 23-005-50 |
00845275005103 | 23-005-47 |
00845275005097 | 23-005-46 |
00845275005080 | 23-005-45 |
00845275005073 | 23-005-44 |
00845275005066 | 23-005-43 |
00845275005042 | 23-005-41 |
00845275005035 | 23-005-40 |
00845275005028 | 23-005-39 |
00845275005011 | 23-005-38 |
00845275005004 | 23-005-37 |
00845275004991 | 23-005-33 |
00845275004984 | 23-005-32 |
00845275004977 | 23-005-31 |
00845275004960 | 23-005-30 |
00845275004953 | 23-005-28 |
00845275004946 | 23-005-27 |
00845275004939 | 23-005-26 |