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Heine Mpack Unplugged Battery

FDA UDI

Class II (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
HEINE MPACK UNPLUGGED BATTERY FDA UDI
Generic Name
Indirect binocular ophthalmoscope FDA UDI
Device Name
HEINE MPACK UNPLUGGED BATTERY WITH MOBILE TRANSFORMER FDA UDI
Model / Reference
X-007.99.666 FDA UDI
Description
HEINE MPACK UNPLUGGED BATTERY WITH MOBILE TRANSFORMER FDA UDI

Identifiers

Primary DI / UDI-DI
00192896009554 FDA UDI
510(k) Number
K142486 FDA UDI
FDA Product Code
HLJ FDA UDI
GMDN Term
Indirect binocular ophthalmoscope FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.1570 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Indirect binocular ophthalmoscope

A comprehensive ophthalmic instrument designed for direct, binocular vision of the eye and surrounding structures. The device features a mobile transformer design, allowing for convenient use in various settings.

Similar devices

Also classified as Indirect binocular ophthalmoscope.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 22291132-c2fd-48ae-8d4a-e103ec161033 35 fields · synced Jul 16, 2026