Primary Device ID | 03760260220316 |
NIH Device Record Key | 953d4e77-a694-4479-8fce-8988b9850c53 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | REFLECTYS |
Version Model Number | P CP |
Catalog Number | CPTYS-P |
Company DUNS | 278261221 |
Company Name | ITENA CLINICAL |
Device Count | 20 |
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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03760260220316 [Primary] |
GS1 | 03760260220538 [Unit of Use] |
EBF | Material, Tooth Shade, Resin |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2022-11-10 |
Device Publish Date | 2016-10-15 |
03760260220316 | P CP |
03760260220309 | I CP |
03760260220293 | E CP |
03760260220286 | A3O CP |
03760260220279 | A2O CP |
03760260220262 | D3 CP |
03760260220255 | C3 CP |
03760260220248 | C2 CP |
03760260220231 | B3 CP |
03760260220224 | B2 CP |
03760260220217 | B1 CP |
03760260220200 | A4 CP |
03760260220194 | A3.5 CP |
03760260220187 | A3 CP |
03760260220170 | A2 CP |
03760260220163 | A1 CP |
03760260220156 | P |
03760260220149 | I |
03760260220132 | E |
03760260220125 | A30 |
03760260220118 | A20 |
03760260220101 | D3 |
03760260220095 | C3 |
03760260220088 | C2 |
03760260220071 | B3 |
03760260220064 | B2 |
03760260220057 | B1 |
03760260220040 | A4 |
03760260220033 | A3.5 |
03760260220026 | A3 |
03760260220019 | A2 |
03760260220002 | A1 |