Cer-View Lateral Wall Retractor (Medium)

GUDID 00888937018035

Cer-View Lateral Wall Retractor (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

Primary Device ID	00888937018035
NIH Device Record Key	a0f8bbb9-f650-43d2-8412-5d0efa23d90a
Commercial Distribution Status	In Commercial Distribution
Brand Name	Cer-View Lateral Wall Retractor (Medium)
Version Model Number	64-310
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	false
RX Perscription	true
OTC Over-The-Counter	false

Device Dimensions

Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter
Width	22 Millimeter
Length	150 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00888937018035 [Primary]

FDA Product Code

HDL	Retractor, Vaginal