Identity
- Trade Name
- Skytron FDA UDI
- Generic Name
- Urological fluid funnel, sterile FDA UDI
- Device Name
- Skytron Urology Drain Bags Vinyl Sterile 13.25in x 33in x 1in 10 per Case FDA UDI
- Model / Reference
- 24606 FDA UDI
- Description
- Skytron Urology Drain Bags Vinyl Sterile 13.25in x 33in x 1in 10 per Case FDA UDI
Identifiers
- Primary DI / UDI-DI
- 01618125157616 FDA UDI
- FDA Product Code
- MMZ FDA UDI
- GMDN Term
- Urological fluid funnel, sterile FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.4890 FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Skytron by Tidi Products, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Tidi Products, Llc
Sources (1)
- FDA UDI 589d5df3-8207-4797-b4b5-27b0166e7c2a 34 fields · synced Jun 6, 2026