Primary Device ID | 13760087126232 |
NIH Device Record Key | 350fb20f-83d9-4a74-917b-53d52bfa8929 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RITLENG PROBE |
Version Model Number | S1.1460 |
Company DUNS | 763408366 |
Company Name | FCI S A S FCI 20 22 |
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 | 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 | 13760087126232 [Primary] |
OKS | Lacrimal Stents And Intubation Sets |
Steralize Prior To Use | true |
Device Is Sterile | false |
[13760087126232]
Moist Heat or Steam Sterilization
[13760087126232]
Moist Heat or Steam Sterilization
[13760087126232]
Moist Heat or Steam Sterilization
[13760087126232]
Moist Heat or Steam Sterilization
[13760087126232]
Moist Heat or Steam Sterilization
[13760087126232]
Moist Heat or Steam Sterilization
[13760087126232]
Moist Heat or Steam Sterilization
[13760087126232]
Moist Heat or Steam Sterilization
[13760087126232]
Moist Heat or Steam Sterilization
[13760087126232]
Moist Heat or Steam Sterilization
[13760087126232]
Moist Heat or Steam Sterilization
[13760087126232]
Moist Heat or Steam Sterilization
[13760087126232]
Moist Heat or Steam Sterilization
[13760087126232]
Moist Heat or Steam Sterilization
[13760087126232]
Moist Heat or Steam Sterilization
[13760087126232]
Moist Heat or Steam Sterilization
[13760087126232]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2023-02-20 |
Device Publish Date | 2021-05-30 |
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