FDA UDI In Commercial Distribution 🇺🇸 United States

SPECTRALIS

DI: 04059237000525 · Model: Software V6.10-US · Heidelberg Engineering GmbH
Product Codes
2
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SPECTRALIS
Primary DI
04059237000525
Version / Model
Software V6.10-US
Company Name
Heidelberg Engineering GmbH
Labeler DUNS
329833875
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-01-03
Public Version
3
Public Version Date
2021-02-19
Public Version Status
Update
Public Device Record Key
756a31b3-98ae-4426-ba6f-59b6776b0553

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
No
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
MYC Ophthalmoscope, Laser, Scanning
OBO Tomography, Optical Coherence

GMDN Terms

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

Identifiers

Type ID
Primary 04059237000525

Premarket Submissions

Submission Number Supplement Number
K173648 000
K181594 000
K182569 000