Primary Device ID | 00840118115964 |
NIH Device Record Key | dc4d6343-cadf-497d-8795-47baf23767de |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MTP Compression Pin Kit, 18mm and 20mm Pins |
Version Model Number | PTK 902 |
Company DUNS | 078790947 |
Company Name | FLOWER ORTHOPEDICS CORPORATION |
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 | 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 |
Phone | 8777788587 |
info@flowerortho.com | |
Phone | 8777788587 |
info@flowerortho.com |
Guidewire Diameter | 1.6 Millimeter |
Length | 160 Millimeter |
Guidewire Diameter | 1.6 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840118115964 [Primary] |
HXI | Passer, Wire, Orthopedic |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-03-05 |
Device Publish Date | 2020-02-26 |
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