Primary Device ID | 20851885004379 |
NIH Device Record Key | 0a9ae072-3b54-4525-8e39-1ac1e4b2757e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ANCHORPORT |
Version Model Number | AP5-135 |
Catalog Number | AP5-135 |
Company DUNS | 071595540 |
Company Name | Conmed Corporation |
Device Count | 3 |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM | |
Phone | +1(800)237-0169 |
CUSTOMER_SERVICE@CONMED.COM |
Length | 135 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 135 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 135 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 135 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 135 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 135 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 135 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 135 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 135 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 135 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 135 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 135 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 135 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 135 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 135 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 135 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 135 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 135 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 135 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00851885004375 [Unit of Use] |
GS1 | 10851885004372 [Primary] |
GS1 | 20851885004379 [Package] Contains: 10851885004372 Package: BOX [3 Units] In Commercial Distribution |
GCJ | Laparoscope, general & plastic surgery |
Steralize Prior To Use | true |
Device Is Sterile | true |
[20851885004379]
Ethylene Oxide
[20851885004379]
Ethylene Oxide
[20851885004379]
Ethylene Oxide
[20851885004379]
Ethylene Oxide
[20851885004379]
Ethylene Oxide
[20851885004379]
Ethylene Oxide
[20851885004379]
Ethylene Oxide
[20851885004379]
Ethylene Oxide
[20851885004379]
Ethylene Oxide
[20851885004379]
Ethylene Oxide
[20851885004379]
Ethylene Oxide
[20851885004379]
Ethylene Oxide
[20851885004379]
Ethylene Oxide
[20851885004379]
Ethylene Oxide
[20851885004379]
Ethylene Oxide
[20851885004379]
Ethylene Oxide
[20851885004379]
Ethylene Oxide
[20851885004379]
Ethylene Oxide
[20851885004379]
Ethylene Oxide
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-01-09 |
Device Publish Date | 2016-09-24 |
20851885004553 | ANCHORPORT 5MM CANNULA WITH INSUFFLATION PORT, 135MM LONG |
20851885004539 | ANCHORPORT 5MM CANNULA WITH INSUFFLATION PORT, 100MM LONG |
20851885004515 | ANCHORPORT 5MM CANNULA WITHOUT INSUFFLATION PORT, 135MM LONG |
20851885004492 | ANCHORPORT 5MM CANNULA WITHOUT INSUFFLATION PORT, 100MM LONG |
20851885004485 | ANCHORPORT 5MM CANNULA WITH INSUFFLATION PORT, 75MM LENGTH |
20851885004454 | ANCHORPORT 5MM CANNULA WITHOUT INSUFFLATION PORT, 75MM LONG |
20851885004430 | ANCHORPORT 5MM SINGLE INCISION LAPAROSCOPY KIT, 135MM LENGTH |
20851885004416 | ANCHORPORT 5MM SINGLE INCISION LAPAROSCOPY KIT, 100MM LENGTH |
20851885004393 | ANCHORPORT 5MM SINGLE INCISION LAPAROSCOPY KIT, 75MM LENGTH |
20851885004379 | ANCHORPORT 5MM TROCAR WITH BLADELESS OPTICAL TIP OBTURATOR AND CANNULA WITH INSUFLATION PORT, 13 |
20851885004355 | ANCHORPORT 5MM TROCAR WITH BLADELESS OPTICAL TIP OBTURATOR AND CANNULA WITH INSUFFLATION PORT, 1 |
20851885004331 | ANCHORPORT 5MM TROCAR WITH BLADELESS OPTICAL TIP OBTURATOR AND CANNULA WITH INSUFFLATION PORT, 7 |
20845854046439 | ANCHORPORT 5MM SINGLE INCISION LAPAROSCOPY KIT, 100MM LENGTH, QTY 6 |
20845854046422 | ANCHORPORT 5MM CANNULA WITH INSUFFLATION PORT, 75MM LENGTH, QTY 12 |
20845854046415 | ANCHORPORT 5MM SINGLE INCISION LAPAROSCOPY KIT, 75MM LENGTH, QTY 6 |
20845854046408 | ANCHORPORT 5MM TROCAR WITH BLADELESS OPTICAL TIP OBTURATOR AND CANNULA WITH INSUFFLATION PORT, 7 |
20845854046392 | ANCHORPORT 5MM TROCAR WITH BLADELESS OPTICAL TIP OBTURATOR AND CANNULA WITH INSUFFLATION PORT, 1 |
20845854046446 | ANCHORPORT 5/100MM INS CANNULA |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ANCHORPORT 77255206 3463852 Live/Registered |
SurgiQuest, Inc. 2007-08-14 |