LEEP Pederson Speculum

GUDID 00888937016093

LEEP Pederson Speculum - Coated - Medium

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	00888937016093
NIH Device Record Key	db3aaf8b-8271-4bb9-9786-19ad6b6c5a2d
Commercial Distribution Status	In Commercial Distribution
Brand Name	LEEP Pederson Speculum
Version Model Number	F221
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	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter
Width	22 Millimeter
Length	114 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00888937016093 [Primary]

FDA Product Code

HDF	Speculum, Vaginal, Metal