Primary Device ID | 10607915117327 |
NIH Device Record Key | a6eb99a9-e184-40b9-be7a-a0d9a5d70cd9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Direct Drive Reposable Scissors |
Version Model Number | CB010 |
Company DUNS | 187129135 |
Company Name | APPLIED MEDICAL RESOURCES CORPORATION |
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 | 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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 1.949.713.8300 |
contact@appliedmedical.com | |
Phone | 1.949.713.8300 |
contact@appliedmedical.com | |
Phone | 1.949.713.8300 |
contact@appliedmedical.com | |
Phone | 1.949.713.8300 |
contact@appliedmedical.com | |
Phone | 1.949.713.8300 |
contact@appliedmedical.com | |
Phone | 1.949.713.8300 |
contact@appliedmedical.com | |
Phone | 1.949.713.8300 |
contact@appliedmedical.com | |
Phone | 1.949.713.8300 |
contact@appliedmedical.com | |
Phone | 1.949.713.8300 |
contact@appliedmedical.com | |
Phone | 1.949.713.8300 |
contact@appliedmedical.com | |
Phone | 1.949.713.8300 |
contact@appliedmedical.com | |
Phone | 1.949.713.8300 |
contact@appliedmedical.com | |
Phone | 1.949.713.8300 |
contact@appliedmedical.com | |
Phone | 1.949.713.8300 |
contact@appliedmedical.com | |
Phone | 1.949.713.8300 |
contact@appliedmedical.com |
Lumen/Inner Diameter | 5 Millimeter |
Lumen/Inner Diameter | 5 Millimeter |
Lumen/Inner Diameter | 5 Millimeter |
Lumen/Inner Diameter | 5 Millimeter |
Length | 34 Centimeter |
Lumen/Inner Diameter | 5 Millimeter |
Length | 34 Centimeter |
Lumen/Inner Diameter | 5 Millimeter |
Length | 34 Centimeter |
Lumen/Inner Diameter | 5 Millimeter |
Length | 34 Centimeter |
Lumen/Inner Diameter | 5 Millimeter |
Length | 34 Centimeter |
Lumen/Inner Diameter | 5 Millimeter |
Length | 34 Centimeter |
Lumen/Inner Diameter | 5 Millimeter |
Length | 34 Centimeter |
Lumen/Inner Diameter | 5 Millimeter |
Length | 34 Centimeter |
Lumen/Inner Diameter | 5 Millimeter |
Length | 34 Centimeter |
Lumen/Inner Diameter | 5 Millimeter |
Length | 34 Centimeter |
Lumen/Inner Diameter | 5 Millimeter |
Length | 34 Centimeter |
Lumen/Inner Diameter | 5 Millimeter |
Length | 34 Centimeter |
Lumen/Inner Diameter | 5 Millimeter |
Length | 34 Centimeter |
Lumen/Inner Diameter | 5 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00607915117320 [Primary] |
GS1 | 10607915117327 [Package] Contains: 00607915117320 Package: [10 Units] In Commercial Distribution |
HET | Laparoscope, Gynecologic (And Accessories) |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-02-21 |
Device Publish Date | 2016-09-24 |
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