Rigid Rat-Tooth Grasping Forceps 4 mm (12 Fr), 37 cm

GUDID 00821925007963

Gyrus Acmi, Inc.

Rigid endoscopic grasping forceps, reusable Rigid endoscopic grasping forceps, reusable Flexible endoscopic biopsy forceps, reusable Flexible endoscopic biopsy forceps, reusable Flexible endoscopic biopsy forceps, reusable Flexible endoscopic biopsy forceps, reusable Flexible endoscopic biopsy forceps, reusable Flexible endoscopic biopsy forceps, reusable Flexible endoscopic biopsy forceps, reusable Flexible endoscopic biopsy forceps, reusable Flexible endoscopic biopsy forceps, reusable Flexible endoscopic biopsy forceps, reusable Flexible endoscopic biopsy forceps, reusable Flexible endoscopic biopsy forceps, reusable Flexible endoscopic biopsy forceps, reusable Flexible endoscopic biopsy forceps, reusable Flexible endoscopic biopsy forceps, reusable
Primary Device ID00821925007963
NIH Device Record Keyba22ebaa-ed22-44d1-aebd-3d9114024eec
Commercial Distribution StatusIn Commercial Distribution
Brand NameRigid Rat-Tooth Grasping Forceps 4 mm (12 Fr), 37 cm
Version Model NumberRRT-437
Company DUNS007198742
Company NameGyrus Acmi, 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 Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100821925007963 [Primary]

FDA Product Code

KOASURGICAL INSTRUMENTS, G-U, MANUAL (AND ACCESSORIES)

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00821925007963]

Moist Heat or Steam Sterilization


[00821925007963]

Moist Heat or Steam Sterilization


[00821925007963]

Moist Heat or Steam Sterilization


[00821925007963]

Moist Heat or Steam Sterilization


[00821925007963]

Moist Heat or Steam Sterilization


[00821925007963]

Moist Heat or Steam Sterilization


[00821925007963]

Moist Heat or Steam Sterilization


[00821925007963]

Moist Heat or Steam Sterilization


[00821925007963]

Moist Heat or Steam Sterilization


[00821925007963]

Moist Heat or Steam Sterilization


[00821925007963]

Moist Heat or Steam Sterilization


[00821925007963]

Moist Heat or Steam Sterilization


[00821925007963]

Moist Heat or Steam Sterilization


[00821925007963]

Moist Heat or Steam Sterilization


[00821925007963]

Moist Heat or Steam Sterilization


[00821925007963]

Moist Heat or Steam Sterilization


[00821925007963]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-10-15
Device Publish Date2018-09-14

Devices Manufactured by Gyrus Acmi, Inc.

00821925041394 - InstaClear2024-04-30 SHEATH, LENS CLEANER ULTRA 0, UNI. LIGHT INSTACLEAR
00821925041400 - InstaClear2024-04-30 SHEATH, LENS CLEANER ULTRA 30DEG, TOP LIGHT INSTACLEAR
00821925041417 - InstaClear2024-04-30 SHEATH LENS CLEANER ULTRA 30DEG, BOTTOM LIGHT INSTACLEAR
00821925041424 - InstaClear2024-04-30 SHEATH, LENS CLEANER ULTRA 45DEG, TOP LIGHT INSTACLEAR
00821925041431 - InstaClear2024-04-30 SHEATH, LENS CLEANER ULTRA 45DEG, BOTTOM LIGHT INSTACLEAR
00821925041448 - InstaClear2024-04-30 SHEATH, LENS CLEANER UNLTRA 70DEG, TOP LIGHT INSTACLEAR
00821925041455 - InstaClear2024-04-30 SHEATH, LENS CLEANER ULTRA 70DEG, BOTTOM LIGHT INSTACLEAR
00810008180983 - nCare2023-10-02 nCare, D, DRCT SDI, ELA, DICOM, RCRDG

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