ALLIGATOR FORCEPS 1271-012Q

GUDID 00192896089419

ALLIGATOR FORCEPS DELICATE TUBULAR SHAFT

SONTEC INSTRUMENTS, INC.

Rigid endoscopic tissue manipulation forceps, reusable
Primary Device ID00192896089419
NIH Device Record Keyea0db1e9-7d92-4b50-8015-89d6828b37f2
Commercial Distribution StatusIn Commercial Distribution
Brand NameALLIGATOR FORCEPS
Version Model Number1271-012Q
Catalog Number1271-012Q
Company DUNS040729840
Company NameSONTEC INSTRUMENTS, 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 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(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com
Phone+1(800) 821-7496
Emailinfo@sontecinstruments.com

Device Dimensions

Device Size Text, specify0
Length6.5 Inch
Device Size Text, specify0
Length6.5 Inch
Device Size Text, specify0
Length6.5 Inch
Device Size Text, specify0
Length6.5 Inch
Device Size Text, specify0
Length6.5 Inch
Device Size Text, specify0
Length6.5 Inch
Device Size Text, specify0
Length6.5 Inch
Device Size Text, specify0
Length6.5 Inch
Device Size Text, specify0
Length6.5 Inch
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896089419 [Primary]

FDA Product Code

FCLFORCEPS, BIOPSY, NON-ELECTRIC

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896089419]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896089419]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896089419]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896089419]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896089419]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896089419]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896089419]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896089419]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896089419]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896089419]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-10-03
Device Publish Date2018-10-24

On-Brand Devices [ALLIGATOR FORCEPS]

00192896089419ALLIGATOR FORCEPS DELICATE TUBULAR SHAFT
00192896079953ALLIGATOR FORCEPS TUNGSTEN CARBIDE DUST SIDE BITING JAW
00192896056312ALLIGATOR FORCEPS DELICATE FLEXIBLE TUBULAR SHAFT
00192896056305ALLIGATOR FORCEPS DELICATE FLEXIBLE TUBULAR SHAFT
00192896056299ALLIGATOR FORCEPS DELICATE FLEXIBLE TUBULAR SHAFT
00192896056282ALLIGATOR FORCEPS DELICATE FLEXIBLE TUBULAR SHAFT
00192896041370ALLIGATOR FORCEPS MICROSCOPIC WITH LOCK SERRATED JAW BLACK ANODIZED COATED
00192896041202ALLIGATOR FORCEPS TUNGSTEN CARBIDE SIDE BITING JAW
00192896041196ALLIGATOR FORCEPS TUNGSTEN CARBIDE SIDE BITING JAW
00192896095472ALLIGATOR FORCEPS TUNGSTEN CARBIDE SERRATED TIP SIDE BITER
00192896093478ALLIGATOR FORCEPS SIDE BITER TUNGSTEN CARBIDE SERRATED TIP

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.