FDA UDI In Commercial Distribution 🇺🇸 United States

HELMUT ZEPF

DI: EZPF41905010 · Model: 41.905.01 · Helmut Zepf Medizintechnik GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HELMUT ZEPF
Primary DI
EZPF41905010
Version / Model
41.905.01
Catalog Number
41.905.01
Company Name
Helmut Zepf Medizintechnik GmbH
Labeler DUNS
320001431
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-07
Public Version
2
Public Version Date
2023-12-12
Public Version Status
Update
Public Device Record Key
37a173a7-71cf-42d9-8fff-ef3f5c09a23a

Device Description

FRACTURE BENDING; FRACTURE WIRE; SPLINTS FRACTURE BENDING = SPLINT HOOKS 1BAR/14CM

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
Yes
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
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
EHO BAR, PREFORMED

GMDN Terms

Code Name
41397 Orthodontic archwire

Identifiers

Type ID
Primary EZPF41905010

Customer Contacts

Phone
+49742498880