Primary Device ID | B286FHCDWC24TSG2201 |
NIH Device Record Key | c1c7b48f-9c14-46c4-a9c6-23f3e926abe2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DUAL CHAMBER WARMING CABINET W/ GLASS DOOR |
Version Model Number | FHCDWC24-TS-G-220 |
Catalog Number | FHCDWC24-TS-G-220 |
Company DUNS | 188660844 |
Company Name | M.A.C. MEDICAL INC. |
Device Count | 1 |
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 | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | (877) 828-9975 |
info@macmedical.com | |
Phone | (877) 828-9975 |
info@macmedical.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B286FHCDWC24TSG2201 [Primary] |
LHC | Warmer, Irrigation Solution |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-07-27 |
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