Identity
- Trade Name
- Weisman Graves Large - Right Side Open FDA UDI
- Generic Name
- Vaginal speculum, reusable FDA UDI
- Device Name
- Weisman Graves Large - Right Side Open 1 3/8" x 4 3/4" (35mm x 121mm) FDA UDI
- Model / Reference
- Weisman Graves Large - Right Side Open 1 3/8" x 4 3/4" (35mm x 121mm) FDA UDI
- Description
- Weisman Graves Large - Right Side Open 1 3/8" x 4 3/4" (35mm x 121mm) FDA UDI
Identifiers
- Catalog Number
- LG030911 FDA UDI
- Primary DI / UDI-DI
- M803LG030911 FDA UDI
- FDA Product Code
- HDF FDA UDI
- GMDN Term
- Vaginal speculum, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 884.4520 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
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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
MR Unsafe FDA UDI
Category: Vaginal speculum, reusable
Weisman Graves Large - Right Side Open by Medgyn Products, Inc. — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Medgyn Products, Inc.
Sources (1)
- FDA UDI 5067f336-29ca-48f0-8775-e7c1e7e974fe 34 fields · synced May 30, 2026