FDA UDI Not in Commercial Distribution 🇺🇸 United States

TWINFIX

DI: 07613153170501 · Model: 92-07211 · 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
07613153170501
Version / Model
92-07211
Catalog Number
92-07211
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
7
Public Version Date
2025-04-14
Public Version Status
Update
Public Device Record Key
1061859d-e965-4e52-bb12-76a549aa385f
Distribution End Date
2022-11-01

Device Description

Sleeve for 07-40210 And 07-40250

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
12143 Instrument tray, reusable

Identifiers

Type ID
Primary 07613153170501

Device Sizes

Type Value Unit Text
Length 18.5 Centimeter