← Back to catalogue

WiFi Kit

FDA UDI

Class I (US FDA UDI)

by Bmc Medical., Ltd.

Identity

Trade Name
WiFi Kit FDA UDI
Generic Name
Home CPAP unit FDA UDI
Device Name
WiFi Kit FDA UDI
Model / Reference
WL-500 FDA UDI
Description
WiFi Kit FDA UDI

Identifiers

Primary DI / UDI-DI
06948538362914 FDA UDI
FDA Product Code
OUG FDA UDI
GMDN Term
Home CPAP unit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6310 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Home CPAP unit

WiFi Kit by Bmc Medical., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Home CPAP unit.

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

Manufacturer
Bmc Medical., Ltd.

Sources (1)

  • FDA UDI 9f67ad59-49b2-482a-aab5-e77060ec7910 33 fields · synced Jun 8, 2026