RELIEVA SIDEKICK LP SDKKLP

GUDID 20705031063546

RELIEVA SIDEKICK SINUS GUIDE HANDLE LOW PROFILE

ACCLARENT, INC.

Paranasal sinus guide-catheter handle
Primary Device ID20705031063546
NIH Device Record Key04418789-b3a4-4514-a423-57f8033d8270
Commercial Distribution StatusIn Commercial Distribution
Brand NameRELIEVA SIDEKICK LP
Version Model NumberSDKKLP
Catalog NumberSDKKLP
Company DUNS361092450
Company NameACCLARENT, INC.
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(877)775-2789
Emailxx@xx.xx

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry place

Device Identifiers

Device Issuing AgencyDevice ID
GS110705031063549 [Primary]
GS120705031063546 [Package]
Contains: 10705031063549
Package: BOX [5 Units]
In Commercial Distribution

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 Date2020-01-22
Device Publish Date2016-10-01

On-Brand Devices [RELIEVA SIDEKICK LP]

20705031131962RELIEVA SIDEKICK SINUS GUIDE HANDLE LOW PROFILE, 1 PK
20705031063546RELIEVA SIDEKICK SINUS GUIDE HANDLE LOW PROFILE

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