Identity
- Trade Name
- LANDANGER FDA UDI
- Generic Name
- Vaginal dilator FDA UDI
- Model / Reference
- F36230 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 03661219069546 FDA UDI
- FDA Product Code
- HDQ FDA UDI
- GMDN Term
- Vaginal dilator FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 884.4530 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
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Vaginal dilator
Landanger by Landanger — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Vaginal dilator.
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- ELMED INCORPORATED — ELMED INCORPORATED · Class I
- DILATOR — KLS-Martin L.P. · Class I
- RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH · Class I
- Novo Surgical Inc. — NOVO SURGICAL, INC. · Class I
- Marina Medical — MARINA MEDICAL INSTRUMENTS, INC. · Class I
- ELMED INCORPORATED — ELMED INCORPORATED · Class I
- GEN2 — SURGIX MEDICAL LLC · Class I
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 I | Pending data |
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Manufacturer
- Manufacturer
- Landanger
Sources (1)
- FDA UDI 05eb3dcc-ee6c-4c4f-bde2-953ef6b672f2 32 fields · synced Jun 8, 2026