RELIEVA SPINPLUS RSP0616MFS

GUDID 20705031232386

RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 6x16 3 GUIDE KIT

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 ID20705031232386
NIH Device Record Keycd552901-80b9-421a-be65-6fbbd5fc07a2
Commercial Distribution StatusIn Commercial Distribution
Brand NameRELIEVA SPINPLUS
Version Model NumberRSP0616MFS
Catalog NumberRSP0616MFS
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(650)687-5888
Emailxx@xx.xx
Phone+1(650)687-5888
Emailxx@xx.xx
Phone+1(650)687-5888
Emailxx@xx.xx
Phone+1(650)687-5888
Emailxx@xx.xx
Phone+1(650)687-5888
Emailxx@xx.xx
Phone+1(650)687-5888
Emailxx@xx.xx
Phone+1(650)687-5888
Emailxx@xx.xx
Phone+1(650)687-5888
Emailxx@xx.xx
Phone+1(650)687-5888
Emailxx@xx.xx
Phone+1(650)687-5888
Emailxx@xx.xx
Phone+1(650)687-5888
Emailxx@xx.xx
Phone+1(650)687-5888
Emailxx@xx.xx
Phone+1(650)687-5888
Emailxx@xx.xx
Phone+1(650)687-5888
Emailxx@xx.xx
Phone+1(650)687-5888
Emailxx@xx.xx
Phone+1(650)687-5888
Emailxx@xx.xx
Phone+1(650)687-5888
Emailxx@xx.xx
Phone+1(650)687-5888
Emailxx@xx.xx
Phone+1(650)687-5888
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
GS110705031232389 [Primary]
GS120705031232386 [Package]
Contains: 10705031232389
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 SPINPLUS]

20705031233062RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 6x16 NO GUIDE KIT, 1 PK
20705031233048RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 5x16 NO GUIDE KIT, 1 PK
20705031232928RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 6x16 M-110C GUIDE KIT, 1 PK
20705031232904RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 6x16 F-70 GUIDE KIT, 1 PK
20705031232867RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 5x16 M-110C GUIDE KIT, 1 PK
20705031232843RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 5x16 F-70 GUIDE KIT, 1 PK
20705031232829RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 5x16 3 GUIDE KIT, 1 PK
20705031232812RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 6x16 3 GUIDE KIT, 1 PK
20705031233055RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 6x16 NO GUIDE KIT
20705031233031RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 5x16 NO GUIDE KIT
20705031232935RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 6x16 M-110C GUIDE KIT
20705031232911RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 6x16 F-70 GUIDE KIT
20705031232874RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 5x16 M-110C GUIDE KIT
20705031232850RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 5x16 F-70 GUIDE KIT
20705031232836RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 5x16 3 GUIDE KIT
20705031232386RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 6x16 3 GUIDE KIT

Trademark Results [RELIEVA SPINPLUS]

Mark Image

Registration | Serial
Company
Trademark
Application Date
RELIEVA SPINPLUS
RELIEVA SPINPLUS
86487044 4886857 Live/Registered
ACCLARENT, INC.
2014-12-19

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