The Stork OTC

GUDID 00810396020090

Conceptive cervical cap, single-use Conceptive cervical cap, single-use

Primary Device ID	00810396020090
NIH Device Record Key	263780bc-71b6-4cf1-841f-6f61c1f0fff9
Commercial Distribution Status	In Commercial Distribution
Brand Name	The Stork OTC
Version Model Number	1000-009
Company DUNS	968804521
Company Name	STORK IB2C, INC., THE
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	true
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	true
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	true
RX Perscription	false
OTC Over-The-Counter	true

Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry
Special Storage Condition, Specify	Between 0 and 0 *Keep Dry

Device Issuing Agency	Device ID
GS1	00810396020090 [Primary]

OBB	Kit, Conception-Assist, Home Use

Steralize Prior To Use	false
Device Is Sterile	true