Primary Device ID | 00813059018458 |
NIH Device Record Key | 846ecce6-aaa7-4341-8c22-235bc3b405f4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Diamatrix Ltd |
Version Model Number | F044-5 |
Catalog Number | F044-5 |
Company DUNS | 809555139 |
Company Name | Diamatrix |
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 | true |
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 | 00813059018458 [Primary] |
HNR | Forceps, Ophthalmic |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00813059018458]
Moist Heat or Steam Sterilization
[00813059018458]
Moist Heat or Steam Sterilization
[00813059018458]
Moist Heat or Steam Sterilization
[00813059018458]
Moist Heat or Steam Sterilization
[00813059018458]
Moist Heat or Steam Sterilization
[00813059018458]
Moist Heat or Steam Sterilization
[00813059018458]
Moist Heat or Steam Sterilization
[00813059018458]
Moist Heat or Steam Sterilization
[00813059018458]
Moist Heat or Steam Sterilization
[00813059018458]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-10-11 |
Device Publish Date | 2022-10-03 |
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