Identity
- Trade Name
- P&P Medical Surgical LLC FDA UDI
- Generic Name
- Vaginal speculum, single-use FDA UDI
- Device Name
- Disposable Vaginal Speculum Light Source Adaptable High Grade Polystyrene Plastic PCS 38% Latex Free Large Size L Pack of 1 FDA UDI
- Model / Reference
- 05600 FDA UDI
- Description
- Disposable Vaginal Speculum Light Source Adaptable High Grade Polystyrene Plastic PCS 38% Latex Free Large Size L Pack of 1 FDA UDI
Identifiers
- Primary DI / UDI-DI
- G026056001 FDA UDI
- FDA Product Code
- HIB FDA UDI
- GMDN Term
- Vaginal speculum, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.4530 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Safe FDA UDI
Category: Vaginal speculum, single-use
P&P Medical Surgical LLC by P&P Medical Surgical LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Vaginal speculum, single-use.
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- Sklar — Sklar Corporation · Class I
- Welch Allyn, Inc. — Welch Allyn, Inc. · 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 |
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Manufacturer
- Manufacturer
- P&P Medical Surgical LLC
Sources (1)
- FDA UDI 22dea40a-b58c-422d-8c89-8b45e110871b 33 fields · synced May 30, 2026