Ambler Surgical 44-505

GUDID 00190660101213

Cohen acorn uterine manipulator, 14 1/2'', includes 1 small and 1 large cervical cones

AMBLER SURGICAL CORP.

Uterine manipulator, reusable
Primary Device ID00190660101213
NIH Device Record Key6ec38ac1-9dbb-45d0-848e-393b7b10014a
Commercial Distribution StatusIn Commercial Distribution
Brand NameAmbler Surgical
Version Model NumberCohen acorn uterine manipulator
Catalog Number44-505
Company DUNS015272206
Company NameAMBLER SURGICAL CORP.
Device Count1
DM Exempttrue
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(888)407-0006
Emailsales@amblersurgical.com
Phone+1(888)407-0006
Emailsales@amblersurgical.com
Phone+1(888)407-0006
Emailsales@amblersurgical.com
Phone+1(888)407-0006
Emailsales@amblersurgical.com
Phone+1(888)407-0006
Emailsales@amblersurgical.com
Phone+1(888)407-0006
Emailsales@amblersurgical.com
Phone+1(888)407-0006
Emailsales@amblersurgical.com
Phone+1(888)407-0006
Emailsales@amblersurgical.com
Phone+1(888)407-0006
Emailsales@amblersurgical.com
Phone+1(888)407-0006
Emailsales@amblersurgical.com
Phone+1(888)407-0006
Emailsales@amblersurgical.com
Phone+1(888)407-0006
Emailsales@amblersurgical.com
Phone+1(888)407-0006
Emailsales@amblersurgical.com
Phone+1(888)407-0006
Emailsales@amblersurgical.com
Phone+1(888)407-0006
Emailsales@amblersurgical.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100190660101213 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GDJCLAMP, SURGICAL, GENERAL & PLASTIC SURGERY

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00190660101213]

Moist Heat or Steam Sterilization


[00190660101213]

Moist Heat or Steam Sterilization


[00190660101213]

Moist Heat or Steam Sterilization


[00190660101213]

Moist Heat or Steam Sterilization


[00190660101213]

Moist Heat or Steam Sterilization


[00190660101213]

Moist Heat or Steam Sterilization


[00190660101213]

Moist Heat or Steam Sterilization


[00190660101213]

Moist Heat or Steam Sterilization


[00190660101213]

Moist Heat or Steam Sterilization


[00190660101213]

Moist Heat or Steam Sterilization


[00190660101213]

Moist Heat or Steam Sterilization


[00190660101213]

Moist Heat or Steam Sterilization


[00190660101213]

Moist Heat or Steam Sterilization


[00190660101213]

Moist Heat or Steam Sterilization


[00190660101213]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-01-15
Device Publish Date2021-01-07

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