FDA UDI In Commercial Distribution 🇺🇸 United States

TrabecuLink Augments - Instruments

DI: 04026575274130 · Model: 185-215/00 · WALDEMAR LINK GmbH & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TrabecuLink Augments - Instruments
Primary DI
04026575274130
Version / Model
185-215/00
Company Name
WALDEMAR LINK GmbH & Co. KG
Labeler DUNS
315675488
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-01-08
Public Version
2
Public Version Date
2026-02-09
Public Version Status
Update
Public Device Record Key
f508f7e3-4b19-446a-a1bf-f37d9894defe

Device Description

Orthopaedic implant impactor - TrabecuLink Augmente

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
HWA Impactor

GMDN Terms

Code Name
32856 Orthopaedic implant impactor, reusable

Identifiers

Type ID
Primary 04026575274130