Identity
- Trade Name
- ONE Vanish FDA UDI
- Generic Name
- Basic male condom, Hevea-latex FDA UDI
- Device Name
- ONE Vanish Backdoor 12-Packs, Case of 18 6 bundles of 3. - specially created for Walmart. 111302C/A- case of 72 of Vanish 12 packs (No inner Bundles) has the same GTIN and will be discontinued. FDA UDI
- Model / Reference
- 11130B2C / 111302C-A FDA UDI
- Description
- ONE Vanish Backdoor 12-Packs, Case of 18 6 bundles of 3. - specially created for Walmart. 111302C/A- case of 72 of Vanish 12 packs (No inner Bundles) has the same GTIN and will be discontinued. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 20726893114726 FDA UDI
- FDA Product Code
- HIS FDA UDI
- GMDN Term
- Basic male condom, Hevea-latex FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.5300 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
Yes
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Basic male condom, Hevea-latex
ONE Vanish by Global Protection Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Basic male condom, Hevea-latex.
- SKORE Smooth Condoms - SKORE (Colors & Flavors) — Ttk Healthcare Limited · Class II
- ID Condoms — WESTRIDGE LABORATORIES INCORPORATED · Class II
- Caliber — Caliber Brand LLC · Class II
- double one — Guangzhou Double One Latex Products Co., Ltd · Class II
- RIDER — SURETEX LIMITED - BRANCH · Class II
- ID Condoms — WESTRIDGE LABORATORIES INCORPORATED · Class II
- LifeStyles Ultra Lubricated 40 ct Bowl — PARADISE MARKETING SERVICES, A CALIFORNIA CORPORATION · Class II
- GETANE — Suzhou Colourway New Material Co., Ltd. · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Global Protection Corp.
Sources (1)
- FDA UDI 208ccaee-9ec0-4378-9e35-b32580242971 34 fields · synced May 30, 2026