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Heine Beta® 200 Led

FDA UDI

Class II (US FDA UDI)

by Heine Optotechnik GmbH & Co. KG

Identity

Trade Name
HEINE BETA® 200 LED FDA UDI
Generic Name
Direct ophthalmoscope FDA UDI
Model / Reference
000 FDA UDI

Identifiers

Catalog Number
C-008.30.100 FDA UDI
Primary DI / UDI-DI
04053755188208 FDA UDI
FDA Product Code
HLJ FDA UDI
GMDN Term
Direct 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Direct ophthalmoscope

Heine Beta® 200 Led by Heine Optotechnik GmbH & Co. KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Direct ophthalmoscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 30cf3379-e804-422b-9c3a-16dbd70271f6 34 fields · synced Jun 1, 2026