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Waveline VS

FDA UDI

Class II (US FDA UDI)

by Avante

Identity

Trade Name
Waveline VS FDA UDI
Generic Name
General-purpose multi-parameter bedside monitor FDA UDI
Model / Reference
60180V FDA UDI

Identifiers

Primary DI / UDI-DI
00815871022156 FDA UDI
510(k) Number
K113653 FDA UDI
FDA Product Code
MHX FDA UDI
FLL FDA UDI
DXN FDA UDI
DSK FDA UDI
DSI FDA UDI
DSA FDA UDI
DRT FDA UDI
DQK FDA UDI
GMDN Term
General-purpose multi-parameter bedside monitor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1025 FDA UDI
880.2910 FDA UDI
870.1130 FDA UDI
870.1110 FDA UDI
870.2900 FDA UDI
870.2300 FDA UDI
870.1425 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

Yes

FDA UDI

Category: General-purpose multi-parameter bedside monitor

Waveline VS by Avante — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose multi-parameter bedside monitor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Avante

Sources (1)

  • FDA UDI c9d3a40d-e75f-4cde-bcbc-777557bca45f 34 fields · synced May 31, 2026