OTOVIEW CUPPED FORCEP JAWS CURVED LEFT 45 DEGREES STAINLESS STEEL EBO

GUDID 00821925026278

Gyrus Acmi, Inc.

Rigid endoscopic grasping forceps, reusable Rigid endoscopic grasping forceps, reusable Rigid endoscopic biopsy forceps, single-use Rigid endoscopic biopsy forceps, single-use Rigid endoscopic biopsy forceps, single-use Rigid endoscopic biopsy forceps, single-use Rigid endoscopic biopsy forceps, single-use Rigid endoscopic biopsy forceps, single-use Rigid endoscopic biopsy forceps, single-use Rigid endoscopic biopsy forceps, single-use Rigid endoscopic biopsy forceps, single-use Rigid endoscopic biopsy forceps, single-use Rigid endoscopic biopsy forceps, single-use Rigid endoscopic biopsy forceps, single-use Rigid endoscopic biopsy forceps, single-use Rigid endoscopic biopsy forceps, single-use Rigid endoscopic biopsy forceps, single-use Rigid endoscopic biopsy forceps, single-use Rigid endoscopic biopsy forceps, single-use Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable Rigid endoscopic tissue manipulation forceps, reusable

Primary Device ID	00821925026278
NIH Device Record Key	f68ccdf2-9061-44e2-be61-1faff0ea3d6c
Commercial Distribution Status	In Commercial Distribution
Brand Name	OTOVIEW CUPPED FORCEP JAWS CURVED LEFT 45 DEGREES STAINLESS STEEL EBO
Version Model Number	70235610
Company DUNS	007198742
Company Name	Gyrus Acmi, Inc.
Device Count	1
DM Exempt	false
Pre-market Exempt	true
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	false
Lot Batch	true
Serial Number	false
Manufacturing Date	true
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00821925026278 [Primary]

FDA Product Code

JXX	FORCEPS, WIRE CLOSURE, ENT, STERILE