← Back to catalogue

Streamway

FDA UDI

Class II (US FDA UDI)

by Skyline Medical Inc.

Identity

Trade Name
Streamway FDA UDI
Generic Name
General-purpose suction system, vacuum FDA UDI
Device Name
Direct to drain liquid fluid waste management system FDA UDI
Model / Reference
4501.3000 FDA UDI
Description
Direct to drain liquid fluid waste management system FDA UDI

Identifiers

Catalog Number
STM 2000 FDA UDI
Primary DI / UDI-DI
10862675000306 FDA UDI
FDA Product Code
GCX FDA UDI
GMDN Term
General-purpose suction system, vacuum 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

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Height — 30 Inch FDA UDI

Category: General-purpose suction system, vacuum

Streamway by Skyline Medical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose suction system, vacuum.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 15d9da6c-6ffa-4028-86cf-2b5774b4101e 36 fields · synced Jun 6, 2026