FDA UDI In Commercial Distribution 🇺🇸 United States

Hahnenkratt

DI: E206542F0 · Model: 542F · E. Hahnenkratt GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Hahnenkratt
Primary DI
E206542F0
Version / Model
542F
Company Name
E. Hahnenkratt GmbH
Labeler DUNS
316001098
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-08-02
Public Version
1
Public Version Date
2024-08-12
Public Version Status
New
Public Device Record Key
9561314a-4508-4326-bb54-ac4c5b8a6d8b

Device Description

ERGOform Explorer Form F pastel blue

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
EKB Explorer, Operative

GMDN Terms

Code Name
35812 Dental surgical probe, reusable

Identifiers

Type ID
Primary E206542F0