Ambler Surgical 20-043

GUDID 00190660024949

Spinal fusion curette, 12'', reverse angled, size #2/0, oval cup, brun handle

AMBLER SURGICAL CORP.

Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable
Primary Device ID00190660024949
NIH Device Record Keyb10d18e0-48ef-4b00-8dc8-a9f548118376
Commercial Distribution StatusIn Commercial Distribution
Brand NameAmbler Surgical
Version Model NumberSpinal fusion curette
Catalog Number20-043
Company DUNS015272206
Company NameAMBLER SURGICAL CORP.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
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
GS100190660024949 [Primary]

FDA Product Code

HAOINSTRUMENT, SURGICAL, NON-POWERED

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00190660024949]

Moist Heat or Steam Sterilization


[00190660024949]

Moist Heat or Steam Sterilization


[00190660024949]

Moist Heat or Steam Sterilization


[00190660024949]

Moist Heat or Steam Sterilization


[00190660024949]

Moist Heat or Steam Sterilization


[00190660024949]

Moist Heat or Steam Sterilization


[00190660024949]

Moist Heat or Steam Sterilization


[00190660024949]

Moist Heat or Steam Sterilization


[00190660024949]

Moist Heat or Steam Sterilization


[00190660024949]

Moist Heat or Steam Sterilization


[00190660024949]

Moist Heat or Steam Sterilization


[00190660024949]

Moist Heat or Steam Sterilization


[00190660024949]

Moist Heat or Steam Sterilization


[00190660024949]

Moist Heat or Steam Sterilization


[00190660024949]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-01-12
Device Publish Date2021-01-04

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