Identity
- Trade Name
- Hope&Her Vaginal Dilators FDA UDI
- Generic Name
- Vaginal dilator FDA UDI
- Device Name
- Hope&Her Vaginal Dilators are indicated to help relieve the symptoms of vaginismus (condition that involves tightening of the vaginal muscles) and related painful sex. The set includes 6 comfortable dilator sizes and an easy-to-attach universal handle. The dilators have a silky-smooth, seamless texture and are not made with BPA, Latex, or silicone. The patented, gentle-tapered design promotes an easy size transition from the smallest size up through the largest. The handle locks on easily and is very study to allow PT muscle manipulation. FDA UDI
- Model / Reference
- T8077 FDA UDI
- Description
- Hope&Her Vaginal Dilators are indicated to help relieve the symptoms of vaginismus (condition that involves tightening of the vaginal muscles) and related painful sex. The set includes 6 comfortable dilator sizes and an easy-to-attach universal handle. The dilators have a silky-smooth, seamless texture and are not made with BPA, Latex, or silicone. The patented, gentle-tapered design promotes an easy size transition from the smallest size up through the largest. The handle locks on easily and is very study to allow PT muscle manipulation. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00860012225002 FDA UDI
- FDA Product Code
- HDX FDA UDI
- GMDN Term
- Vaginal dilator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.3900 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Vaginal dilator
Hope&Her Vaginal Dilators by Lujena, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 |
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Manufacturer
- Manufacturer
- Lujena, Inc.
Sources (1)
- FDA UDI 7849694c-e2bf-4b50-9744-f762e686e8ec 35 fields · synced May 31, 2026