Primary Device ID | B470PEZ1920201 |
NIH Device Record Key | b2aa5b16-3049-4d18-bf13-66ee2bb72e03 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Compressyn Staple |
Version Model Number | PEZ-192020 |
Catalog Number | PEZ-192020 |
Company DUNS | 010690010 |
Company Name | DALLEN 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 | true |
Device Combination Product | false |
Single Use | true |
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 |
---|---|
HIBCC | B470PEZ1920201 [Primary] |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-05-07 |
Device Publish Date | 2016-11-02 |
00850815007134 | PEZ-130907 |
00850815007127 | PEZ-131110 |
00850815007110 | PEZ-131115 |
00850815007103 | PEZ-131117 |
00850815007097 | PEZ-131119 |
00850815007080 | PEZ-131310 |
00850815007073 | PEZ-131512 |
00850815007066 | PEZ-191512 |
00850815007059 | PEZ-191518 |
00850815007042 | PEZ-191818 |
00850815007035 | PEZ-192020 |
00850815007028 | PEZ-242020 |
00850815007011 | PEZ-242522 |
00850815007004 | PEZ-243030 |
B470PEZ2430301 | PEZ-243030 |
B470PEZ2425221 | PEZ-242522 |
B470PEZ2420201 | PEZ-242020 |
B470PEZ1920201 | PEZ-192020 |
B470PEZ1918181 | PEZ-191818 |
B470PEZ1915181 | PEZ-191518 |
B470PEZ1915121 | PEZ-191512 |
B470PEZ1315121 | PEZ-131512 |
B470PEZ1313101 | PEZ-131310 |
B470PEZ1311191 | PEZ-131119 |
B470PEZ1311171 | PEZ-131117 |
B470PEZ1311151 | PEZ-131115 |
B470PEZ1311101 | PEZ-131110 |
B470PEZ1309071 | PEZ-130907 |