FDA UDI In Commercial Distribution 🇺🇸 United States

Oertli®

DI: 07630003901382 · Model: VE820003 · Oertli-Instrumente AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Oertli®
Primary DI
07630003901382
Version / Model
VE820003
Company Name
Oertli-Instrumente AG
Labeler DUNS
481505238
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-19
Public Version
10
Public Version Date
2022-09-16
Public Version Status
Update
Public Device Record Key
de2a0071-baea-4404-a3db-71c7581a2fd1

Device Description

CATARHEX TRAG-KOFFER ; CATARHEX CARRYING CASE; CATARHEX VALISE "PILOTE"

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
No
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
12143 Instrument tray, reusable

Identifiers

Type ID
Primary 07630003901382

Customer Contacts

Phone
+41717474200