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Onera STS

FDA UDI

Class II (US FDA UDI)

by Onera B.V.

Identity

Trade Name
Onera STS FDA UDI
Generic Name
Polysomnography analyser FDA UDI
Model / Reference
01.00 FDA UDI

Identifiers

Catalog Number
ONERA STS1 HEAD CRADLE FDA UDI
Primary DI / UDI-DI
08720256698029 FDA UDI
510(k) Number
K210593 FDA UDI
FDA Product Code
MNR FDA UDI
OLV FDA UDI
GMDN Term
Polysomnography analyser FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.2375 FDA UDI
882.1400 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

No

FDA UDI

Dimensions & Sizes

Size
Weight — 293 Gram FDA UDI
Length — 160 Millimeter FDA UDI
Width — 80 Millimeter FDA UDI
Height — 86 Millimeter FDA UDI

Category: Polysomnography analyser

Onera STS by Onera B.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polysomnography analyser.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Onera B.V.

Sources (1)

  • FDA UDI a0003c4e-60dd-46e0-8925-46ecfad897ea 37 fields · synced Jun 6, 2026