FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10886982311535 · Model: SD391.931 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
NA
Primary DI
10886982311535
Version / Model
SD391.931
Catalog Number
SD391931
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-05-29
Public Version
2
Public Version Date
2026-04-06
Public Version Status
Update
Public Device Record Key
67e6b025-ab4d-4fdd-8a22-09865411f8e2

Device Description

TIGHTENING CAP ASSEMBLY K-WIRE CUTTER

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
HXZ CUTTER, WIRE

GMDN Terms

Code Name
44805 Orthopaedic implantable-device cutter

Identifiers

Type ID
Primary 10886982311535

Customer Contacts