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Qosmic

FDA UDI

Class I (US FDA UDI)

by Enova Illumination, Inc

Identity

Trade Name
QOSMIC FDA UDI
Generic Name
Portable/mobile rechargeable battery pack FDA UDI
Device Name
QOSMIC™ Battery Pack FDA UDI
Model / Reference
5460-800-009 FDA UDI
Description
QOSMIC™ Battery Pack FDA UDI

Identifiers

Primary DI / UDI-DI
00850025993883 FDA UDI
FDA Product Code
HPP FDA UDI
GMDN Term
Portable/mobile rechargeable battery pack FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4335 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Portable/mobile rechargeable battery pack

Qosmic by Enova Illumination, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Portable/mobile rechargeable battery pack.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 23afeb8c-c1b9-4130-ac61-415cae243769 33 fields · synced May 30, 2026