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Meniett™ Battery Pack, 9.6 VDC

FDA UDI

Class II (US FDA UDI)

by Lina Medical ApS

Identity

Trade Name
Meniett™ Battery Pack, 9.6 VDC FDA UDI
Generic Name
Primary battery FDA UDI
Model / Reference
MT-BATT FDA UDI

Identifiers

Catalog Number
MT-BATT FDA UDI
Primary DI / UDI-DI
05708265004935 FDA UDI
FDA Product Code
ETY FDA UDI
GMDN Term
Primary battery FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.1090 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Primary battery

Meniett™ Battery Pack, 9.6 VDC by Lina Medical ApS — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Primary battery.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Lina Medical ApS

Sources (1)

  • FDA UDI bc5d6eae-7b27-4da1-a7a7-b5563e53e6bc 34 fields · synced May 30, 2026