FDA UDI In Commercial Distribution 🇺🇸 United States

SPECTRALIS

DI: 04059237000235 · Model: 86549 · Heidelberg Engineering GmbH
Product Codes
2
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
SPECTRALIS
Primary DI
04059237000235
Version / Model
86549
Catalog Number
86549
Company Name
Heidelberg Engineering GmbH
Labeler DUNS
329833875
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-03-24
Public Version
2
Public Version Date
2026-04-13
Public Version Status
Update
Public Device Record Key
810a9e3d-5e7e-4733-a8dd-894827d6e344

Device Description

Flex Module

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
OBO Tomography, Optical Coherence
MYC Ophthalmoscope, Laser, Scanning

GMDN Terms

Code Name
47952 Scanning-laser retinal imaging system
58850 Ophthalmic spectral-domain optical coherence tomography system

Identifiers

Type ID
Primary 04059237000235

Premarket Submissions

Submission Number Supplement Number
K241163 000