Identity
- Trade Name
- Realstar Surgical FDA UDI
- Generic Name
- Post-parturition vaginal retractor FDA UDI
- Device Name
- Rigby Retractor FDA UDI
- Model / Reference
- RSSI-130-150 FDA UDI
- Description
- Rigby Retractor FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00850071684254 FDA UDI
- FDA Product Code
- HDL FDA UDI
- GMDN Term
- Post-parturition vaginal retractor 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
Category: Post-parturition vaginal retractor
Realstar Surgical by Real Star Surgical Instruments — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Post-parturition vaginal retractor.
- Hegenberger Medical — HEGENBERGER MEDICAL LIMITED · Class I
- Soviflex — Birch Concepts 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Real Star Surgical Instruments
Sources (1)
- FDA UDI 665a3ca4-1f4f-4f63-ba63-7ef597a40f67 33 fields · synced Jun 8, 2026