FDA UDI In Commercial Distribution 🇺🇸 United States

n/a

DI: E0HM39HI0121 · Model: HI012 · Hager & Meisinger Gesellschaft mit beschränkter Haftung
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
n/a
Primary DI
E0HM39HI0121
Version / Model
HI012
Catalog Number
HI012
Company Name
Hager & Meisinger Gesellschaft mit beschränkter Haftung
Labeler DUNS
318034329
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-09-15
Public Version
2
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
657632e7-7bf4-4726-8539-5f0cf2b27869

Device Description

Manual instrument for dental/surgical application

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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
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
DZN INSTRUMENTS, DENTAL HAND

GMDN Terms

Code Name
35559 Bone file/rasp, manual, reusable

Identifiers

Type ID
Primary E0HM39HI0121

Customer Contacts