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Heine Mpack Complete

FDA UDI

Class II (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
HEINE MPACK COMPLETE FDA UDI
Generic Name
Indirect binocular ophthalmoscope FDA UDI
Device Name
HEINE MPACK COMPLETE WITH TRANSFORMER FDA UDI
Model / Reference
X-007.99.672 FDA UDI
Description
HEINE MPACK COMPLETE WITH TRANSFORMER FDA UDI

Identifiers

Primary DI / UDI-DI
00192896009585 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
Sterilization Method
Dry Heat Sterilization FDA UDI

Category: Indirect binocular ophthalmoscope

Heine Mpack Complete by Sontec Instruments, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 b5d7198a-c11a-4c1f-afe0-4bea721a765a 35 fields · synced May 30, 2026