Salman FES Stent SS2000

GUDID EBESSS20000

BOSTON MEDICAL PRODUCTS, INC.

Paranasal sinus spacer Paranasal sinus spacer Paranasal sinus spacer Paranasal sinus spacer Paranasal sinus spacer Paranasal sinus spacer Paranasal sinus spacer Paranasal sinus spacer Paranasal sinus spacer Paranasal sinus spacer Paranasal sinus spacer Paranasal sinus spacer Paranasal sinus spacer Paranasal sinus spacer Paranasal sinus spacer
Primary Device IDEBESSS20000
NIH Device Record Key14d53864-efa7-48c0-a0e6-1a696dff8cfa
Commercial Distribution StatusIn Commercial Distribution
Brand NameSalman FES Stent
Version Model NumberSS2000
Catalog NumberSS2000
Company DUNS131855157
Company NameBOSTON MEDICAL PRODUCTS, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Safe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1-800-433-2674
Emailinfo@bosmed.com
Phone1-800-433-2674
Emailinfo@bosmed.com
Phone1-800-433-2674
Emailinfo@bosmed.com
Phone1-800-433-2674
Emailinfo@bosmed.com
Phone1-800-433-2674
Emailinfo@bosmed.com
Phone1-800-433-2674
Emailinfo@bosmed.com
Phone1-800-433-2674
Emailinfo@bosmed.com
Phone1-800-433-2674
Emailinfo@bosmed.com
Phone1-800-433-2674
Emailinfo@bosmed.com
Phone1-800-433-2674
Emailinfo@bosmed.com
Phone1-800-433-2674
Emailinfo@bosmed.com
Phone1-800-433-2674
Emailinfo@bosmed.com
Phone1-800-433-2674
Emailinfo@bosmed.com
Phone1-800-433-2674
Emailinfo@bosmed.com
Phone1-800-433-2674
Emailinfo@bosmed.com

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCEBESSS20000 [Primary]
HIBCCEBESSS20001 [Package]
Package: Carton [1 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KAMCannula, Sinus

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2018-10-05
Device Publish Date2015-09-20

On-Brand Devices [Salman FES Stent]

EBESSS20000SS2000
34063107102159SS2000

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