RELIEVA SPIN RSS0

GUDID 20705031206028

RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, S-0 SINUS GUIDE CATHETER TIP

ACCLARENT, INC.

Epistaxsis balloon Epistaxis balloon Epistaxis balloon Epistaxis balloon Epistaxis balloon Epistaxis balloon Epistaxis balloon Epistaxis balloon Epistaxis balloon Epistaxis balloon Epistaxis balloon Nasal haemostatic balloon Nasal haemostatic balloon Nasal haemostatic balloon Nasal haemostatic balloon Nasal haemostatic balloon Nasal haemostatic balloon Nasal haemostatic balloon Nasal haemostatic balloon
Primary Device ID20705031206028
NIH Device Record Keydedf35e5-ccc7-4904-9a56-67a2432251ca
Commercial Distribution StatusIn Commercial Distribution
Brand NameRELIEVA SPIN
Version Model NumberRSS0
Catalog NumberRSS0
Company DUNS361092450
Company NameACCLARENT, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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
Phone+1(877)775-2789
Emailxx@xx.xx
Phone+1(877)775-2789
Emailxx@xx.xx
Phone+1(877)775-2789
Emailxx@xx.xx
Phone+1(877)775-2789
Emailxx@xx.xx
Phone+1(877)775-2789
Emailxx@xx.xx
Phone+1(877)775-2789
Emailxx@xx.xx
Phone+1(877)775-2789
Emailxx@xx.xx
Phone+1(877)775-2789
Emailxx@xx.xx
Phone+1(877)775-2789
Emailxx@xx.xx
Phone+1(877)775-2789
Emailxx@xx.xx
Phone+1(877)775-2789
Emailxx@xx.xx
Phone+1(877)775-2789
Emailxx@xx.xx
Phone+1(877)775-2789
Emailxx@xx.xx
Phone+1(877)775-2789
Emailxx@xx.xx
Phone+1(877)775-2789
Emailxx@xx.xx
Phone+1(877)775-2789
Emailxx@xx.xx
Phone+1(877)775-2789
Emailxx@xx.xx
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
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry place
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool, dry place

Device Identifiers

Device Issuing AgencyDevice ID
GS110705031206021 [Primary]
GS120705031206028 [Package]
Contains: 10705031206021
Package: BOX [5 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LRCINSTRUMENT, ENT MANUAL SURGICAL

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 SPIN]

20705031230580RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, 6x16 3 GUIDE KIT, 1 PK
20705031230566RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, 5x16 3 GUIDE KIT, 1 PK
20705031227580RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, M-110C SINUS GUIDE CATHETER TIP, 1 PK
20705031206370RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, 5x16 F-70 GUIDE KIT, 1 PK
20705031206325RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, 5x16 M-110C GUIDE KIT, 1 PK
20705031206042RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, M-110 SINUS GUIDE CATHETER TIP, 1 PK
20705031206011RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, S-0 SINUS GUIDE CATHETER TIP, 1 PK
20705031200576RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, 6x16 M-110 GUIDE KIT, 1 PK
20705031200545RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, 6x16 F-70 GUIDE KIT, 1 PK
20705031200538RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, F-70 SINUS GUIDE CATHETER TIP, 1 PK
20705031230597RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, 6x16 3 GUIDE KIT
20705031230573RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, 5x16 3 GUIDE KIT
20705031227573RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, M-110C SINUS GUIDE CATHETER TIP
20705031206318RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, 5x16 M-110C GUIDE KIT
20705031206301RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, 5x16 F-70 GUIDE KIT
20705031206035RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, M-110 SINUS GUIDE CATHETER TIP
20705031206028RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, S-0 SINUS GUIDE CATHETER TIP
20705031200583RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, F-70 SINUS GUIDE CATHETER TIP
20705031200569RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, 6x16 M-110 GUIDE KIT
20705031200552RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, 6x16 F-70 GUIDE KIT

Trademark Results [RELIEVA SPIN]

Mark Image

Registration | Serial
Company
Trademark
Application Date
RELIEVA SPIN
RELIEVA SPIN
85436310 4335661 Dead/Cancelled
ACCLARENT, INC.
2011-09-30

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