FDA UDI In Commercial Distribution 🇺🇸 United States

Oertli®

DI: 07630003920178 · Model: VE820006 · Oertli-Instrumente AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Oertli®
Primary DI
07630003920178
Version / Model
VE820006
Company Name
Oertli-Instrumente AG
Labeler DUNS
481505238
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-09-19
Public Version
1
Public Version Date
2025-09-29
Public Version Status
New
Public Device Record Key
f7beb3ef-f9de-4f4c-8926-bd5871afc332

Device Description

Infusion Cart CataRhex 3

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
HQC Unit, Phacofragmentation

GMDN Terms

Code Name
46433 Ophthalmic instrument table, manual

Identifiers

Type ID
Primary 07630003920178

Customer Contacts

Phone
+41717474200