FDA UDI In Commercial Distribution 🇺🇸 United States

The Stork OTC

DI: 00810396020090 · Model: 1000-009 · STORK IB2C, INC., THE
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
The Stork OTC
Primary DI
00810396020090
Version / Model
1000-009
Company Name
STORK IB2C, INC., THE
Labeler DUNS
968804521
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-10-11
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
263780bc-71b6-4cf1-841f-6f61c1f0fff9

Device Description

The Stork, UK

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OBB Kit, Conception-Assist, Home Use

GMDN Terms

Code Name
61449 Conceptive cervical cap, single-use

Identifiers

Type ID
Primary 00810396020090

Customer Contacts

Phone
412-200-7996

Premarket Submissions

Submission Number Supplement Number
K140186 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-30 – 54 Degrees Celsius
Type
Special Storage Condition, Specify
Special Conditions
Keep away from sunlight
Type
Special Storage Condition, Specify
Special Conditions
Keep Dry