Identity
- Trade Name
- Precision S 4K FDA UDI
- Generic Name
- Rigid optical rhinoscope FDA UDI
- Model / Reference
- 0502-655-010 FDA UDI
Identifiers
- Catalog Number
- 0502-655-010 FDA UDI
- Primary DI / UDI-DI
- 07613327412161 FDA UDI
- FDA Product Code
- EOB FDA UDI
- GMDN Term
- Rigid optical rhinoscope FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 874.4760 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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Angle — 0.0 degree FDA UDILength — 180.0 Millimeter FDA UDI
Category: Rigid optical rhinoscope
Precision S 4K by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Rigid optical rhinoscope.
- HOPKINS — Karl Storz GmbH & Co. KG · Class II
- HOPKINS — Karl Storz GmbH & Co. KG · Class II
- HOPKINS — Karl Storz GmbH & Co. KG · Class II
- HOPKINS — Karl Storz GmbH & Co. KG · Class II
- Olympus — Olympus Winter & Ibe GmbH · Class II
- HOPKINS — Karl Storz GmbH & Co. KG · Class II
- HOPKINS — Karl Storz GmbH & Co. KG · Class II
- Olympus — Olympus Winter & Ibe GmbH · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Stryker Corp.
Sources (1)
- FDA UDI a2b078d4-29da-4491-8b5a-28521512177c 35 fields · synced May 30, 2026