Primary Device ID | 10816505020736 |
NIH Device Record Key | b5a2368e-b0a0-4a3f-aa95-4e8638490198 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Cramer Decker Medical |
Version Model Number | AREG8708 |
Company DUNS | 041036187 |
Company Name | Cramer Decker Medical |
Device Count | 1 |
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 | 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 | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00816505020739 [Primary] |
GS1 | 10816505020736 [Package] Contains: 00816505020739 Package: [20 Units] In Commercial Distribution |
CAN | Regulator, Pressure, Gas Cylinder |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-02-08 |
Device Publish Date | 2022-01-31 |
10816505020767 | AREG8725-B2D |
10816505020750 | AREG8715ME |
10816505020743 | AREG8715 |
10816505020736 | AREG8708 |
10816505020712 | AREG8704-GREEN-PROMOLIFE |
10816505020705 | AREG8704 |
10816505020699 | AREG5415 |
10816505020682 | AREG5408 |
10816505020675 | AREG5404-SILVER-PROMOLIFE |
10816505020668 | AREG5404-NS-BLUE-PROMOLIFE |
10816505020651 | AREG5404-BU-BAAD |
10816505020644 | AREG5404 |