FDA UDI In Commercial Distribution 🇺🇸 United States

BEYOND SEVEN® Studded Condoms

DI: 00028373520123 · Model: 52012 · OKAMOTO USA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
12

Basic Information

Brand Name
BEYOND SEVEN® Studded Condoms
Primary DI
00028373520123
Version / Model
52012
Catalog Number
52012
Company Name
OKAMOTO USA, INC.
Labeler DUNS
175752724
Distribution Status
In Commercial Distribution
Device Count in Pkg
12
Record Status
Published
Publish Date
2016-09-22
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
06530201-6e94-4c0a-b3f7-295f8b3b31b2

Device Description

Natural rubber latex condom, lubricated, studded.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
Yes
Not Made with NRL
No
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
HIS Condom

GMDN Terms

Code Name
45138 Basic male condom, Hevea-latex

Identifiers

Type ID
Package 10028373520120
Primary 00028373520123
Unit of Use 80028373520129

Customer Contacts