FDA UDI In Commercial Distribution 🇺🇸 United States

MMF AXS

DI: 07613327581812 · Model: 01-03019 · Stryker Leibinger GmbH & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MMF AXS
Primary DI
07613327581812
Version / Model
01-03019
Catalog Number
01-03019
Company Name
Stryker Leibinger GmbH & Co. KG
Labeler DUNS
316153956
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-09-15
Public Version
1
Public Version Date
2023-09-25
Public Version Status
New
Public Device Record Key
65d8478a-acc7-4ca3-8d31-b0c802a35060

Device Description

AXS Tension Sheath, MMF, spare

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
LXH Orthopedic manual surgical instrument

GMDN Terms

Code Name
44054 Orthopaedic surgical procedure kit, non-medicated, reusable

Identifiers

Type ID
Primary 07613327581812

Device Sizes

Type Value Unit Text
Length 44.0 Millimeter