FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 37613153045572 · Model: 81-03403 · Stryker Leibinger GmbH & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
NA
Primary DI
37613153045572
Version / Model
81-03403
Catalog Number
81-03403
Company Name
Stryker Leibinger GmbH & Co. KG
Labeler DUNS
316153956
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2016-08-24
Public Version
3
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
f921ade6-62d0-47dd-9b3f-81e0baed1453

Device Description

BONE SCREWS, EMERG., CROSS-FIT,SELF-TAPP

Device Characteristics

Single Use
Yes
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
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
HAW Neurological stereotaxic Instrument

GMDN Terms

Code Name
56642 Orthopaedic bone screw, non-bioabsorbable, non-sterile

Identifiers

Type ID
Primary 37613153045572
Unit of Use 07613153045571

Device Sizes

Type Value Unit Text
Length 4.5 Millimeter
Device Size Text, specify Diameter: 2.3 Millimeter