LEEP Jackson Retractor

GUDID 00888937016178

LEEP Jackson Retractor - Coated- Large

Coopersurgical, Inc.

Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable Vaginal speculum, reusable

Primary Device ID	00888937016178
NIH Device Record Key	687de633-6843-40b6-8244-e7891d15000f
Commercial Distribution Status	In Commercial Distribution
Brand Name	LEEP Jackson Retractor
Version Model Number	F234
Company DUNS	801895244
Company Name	Coopersurgical, 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	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	true
RX Perscription	true
OTC Over-The-Counter	false

Device Dimensions

Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter
Width	40 Millimeter
Length	115 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00888937016178 [Primary]

FDA Product Code

HDF	Speculum, Vaginal, Metal