Primary Device ID | 00614950029792 |
NIH Device Record Key | 5544dd10-dae3-48fd-a6ea-86d529c91e52 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ELEVATOR |
Version Model Number | 0000220 |
Catalog Number | 0000220 |
Company DUNS | 042763706 |
Company Name | ACE SURGICAL SUPPLY CO., INC. |
Device Count | 1 |
DM Exempt | true |
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 | false |
Manufacturing Date | false |
Expiration Date | false |
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 | 00614950029792 [Primary] |
EMJ | ELEVATOR, SURGICAL, DENTAL |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-12-13 |
Device Publish Date | 2023-12-05 |
00614950029952 | PERIOSTEAL MOLT D/E S/B 7-1/2” 19CM |
00614950029945 | PERIOSTEAL MOLT #9 HEAVY 7-1/2" 19CM |
00614950029792 | ELEVATOR ANTRALPLASTY KIT SET OF 6 INSTRUMENTS |