FDA UDI
In Commercial Distribution
🇺🇸 United States
Restore Moisturizing Vaginal Gel
DI: 00893268000222
·
Model: 2oz.
·
GOOD CLEAN LOVE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
1
Basic Information
- Brand Name
- Restore Moisturizing Vaginal Gel
- Primary DI
- 00893268000222
- Version / Model
- 2oz.
- Catalog Number
- 500102
- Company Name
- GOOD CLEAN LOVE, INC.
- Labeler DUNS
- 153909531
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2017-09-25
- Public Version
- 8
- Public Version Date
- 2023-12-11
- Public Version Status
- Update
- Public Device Record Key
- c156373b-c3bb-4618-918c-82cc43a0ec60
Device Description
Restore is a personal lubricant for penile and/or vaginal application intended to moisturize and lubricate, to enhance the ease and comfort of intimate sexual activity and supplement the body's natural lubrication. This product is compatible with natural rubber latex and polyisoprene condoms. It is not compatible with polyurethane condoms.
Device Characteristics
- Single Use
- Yes
- Prescription Use (Rx)
- No
- Over the Counter (OTC)
- Yes
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- 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 | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| NUC | Lubricant, Personal | Obstetrics/Gynecology | 884.5300 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 60412 | Sexual lubricant | A substance (e.g., a gel or jelly) intended to be applied to the penis, vagina and/or anus for lubrication during sexual intercourse or to be used with a sexual vibrator. This substance contains no pharmaceutical ingredients. After application, this device cannot be reused. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 00893268000222 | GS1 | ||||
| Package | 30893268000742 | GS1 | Master Case | 24 | In Commercial Distribution | |
| Package | 40893268000220 | GS1 | Master Case | 24 | In Commercial Distribution | |
| Package | 50893268000227 | GS1 | Master Case | 96 | In Commercial Distribution |
Customer Contacts
- Phone
- 541-344-4483
- [email protected]
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K162207 | 000 |