Primary Device ID | 10810090011438 |
NIH Device Record Key | c23567a3-7447-4282-ab9d-a351e77d07a8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | N/A |
Version Model Number | 810-21 |
Company DUNS | 555862549 |
Company Name | Eagle Labs |
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 | true |
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 | 909-481-0011 |
eaglelabs@eaglelabs.com | |
Phone | 909-481-0011 |
eaglelabs@eaglelabs.com |
Area/Surface Area | 256 Square inch |
Area/Surface Area | 256 Square inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00810090011431 [Primary] |
GS1 | 10810090011438 [Package] Contains: 00810090011431 Package: carton [10 Units] In Commercial Distribution |
HMT | Drape, Patient, Ophthalmic |
Steralize Prior To Use | true |
Device Is Sterile | true |
[10810090011438]
Ethylene Oxide
[10810090011438]
Ethylene Oxide
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-10-28 |
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