FDA UDI In Commercial Distribution 🇺🇸 United States

Intramedullary Plugs

DI: 04026575230884 · Model: 109-130/13 · WALDEMAR LINK GmbH & Co. KG
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Intramedullary Plugs
Primary DI
04026575230884
Version / Model
109-130/13
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
2025-11-24
Public Version
1
Public Version Date
2025-12-02
Public Version Status
New
Public Device Record Key
1bd47f24-8785-477b-9f75-64d8825ab1c1

Device Description

Intramedullary Plug, Ø13 mm

Device Characteristics

Single Use
Yes
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
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
OQG Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented
KWY Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented
MEH Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate

GMDN Terms

Code Name
38799 Polymer orthopaedic cement restrictor, non-bioabsorbable

Identifiers

Type ID
Primary 04026575230884

Premarket Submissions

Submission Number Supplement Number
K250375 000