Identity
- Trade Name
- Streamway Filter FDA UDI
- Generic Name
- Suction system filter, tissue, non-sterile FDA UDI
- Device Name
- Procedure Filter for Streamway device FDA UDI
- Model / Reference
- STM 2015 FDA UDI
- Description
- Procedure Filter for Streamway device FDA UDI
Identifiers
- Catalog Number
- STM 2015 FDA UDI
- Primary DI / UDI-DI
- 10862675000313 FDA UDI
- FDA Product Code
- GCX FDA UDI
- GMDN Term
- Suction system filter, tissue, non-sterile FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6740 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
MR Safe FDA UDI
Category: Suction system filter, tissue, non-sterile
Streamway Filter by Skyline Medical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Suction system filter, tissue, non-sterile.
- EndoRotor® Filter Set — INTERSCOPE, 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Skyline Medical Inc.
Sources (1)
- FDA UDI 3eeafd93-05e0-4a08-a8d9-5d6bdcef5bbd 35 fields · synced May 30, 2026