Primary Device ID | 00854258006204 |
NIH Device Record Key | fcda9f42-e553-4ff6-81b9-5b964e081b0d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CovoraTM |
Version Model Number | COV1-5X5 |
Company DUNS | 040631370 |
Company Name | ACERA SURGICAL INC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | true |
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 |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Width | 5 Centimeter |
Length | 5 Centimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00854258006204 [Primary] |
FRO | Dressing, Wound, Drug |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-11-11 |
Device Publish Date | 2019-10-04 |
00854258006228 | CovoraTM is a sterile,single use device intended for use in partial thickness burns. CovoraTM is |
00854258006211 | CovoraTM is a sterile,single use device intended for use in partial thickness burns. CovoraTM is |
00854258006204 | CovoraTM is a sterile,single use device intended for use in partial thickness burns. CovoraTM is |