FDA UDI Not in Commercial Distribution 🇺🇸 United States

Screwdriver

DI: E219J531605041 · Model: J5316.0504 · ALTATEC GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Screwdriver
Primary DI
E219J531605041
Version / Model
J5316.0504
Catalog Number
J5316.0504
Company Name
ALTATEC GmbH
Labeler DUNS
322018193
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-12-31
Public Version
2
Public Version Date
2023-06-16
Public Version Status
Update
Public Device Record Key
eaf8dff1-5b6e-4cae-b1e7-40a08508cc35
Distribution End Date
2023-06-15

Device Description

Screwdriver, hex, short, ISO shaft

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
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
NDP Accessories, Implant, Dental, Endosseous

GMDN Terms

Code Name
33968 Surgical screwdriver, reusable

Identifiers

Type ID
Primary E219J531605041

Customer Contacts

Phone
9999999999