FDA UDI In Commercial Distribution 🇺🇸 United States

Bikini

DI: 08859798105020 · Model: 08859798105020 · SURETEX LIMITED - BRANCH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Bikini
Primary DI
08859798105020
Version / Model
08859798105020
Company Name
SURETEX LIMITED - BRANCH
Labeler DUNS
672044515
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-07-30
Public Version
1
Public Version Date
2025-08-07
Public Version Status
New
Public Device Record Key
9b9b5b5f-0383-4e12-b994-3f3deac54b9b

Device Description

Bikini CONDOM 1ct

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
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
Primary 08859798105020

Premarket Submissions

Submission Number Supplement Number
K941258 000