FDA UDI Not in Commercial Distribution 🇺🇸 United States

TWINFIX

DI: 04546540361998 · Model: 07-40232 · Stryker GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
TWINFIX
Primary DI
04546540361998
Version / Model
07-40232
Catalog Number
07-40232
Company Name
Stryker GmbH
Labeler DUNS
481999654
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-24
Public Version
4
Public Version Date
2025-04-14
Public Version Status
Update
Public Device Record Key
2d23ba58-4cb0-48ea-8bdd-28c54217cf1b
Distribution End Date
2022-11-01

Device Description

Cannulated Tap

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
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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
56708 Bone tap, single-use

Identifiers

Type ID
Primary 04546540361998

Device Sizes

Type Value Unit Text
Length 155.0 Millimeter
Device Size Text, specify Diameter: 3.2 Millimeter