FDA UDI In Commercial Distribution 🇺🇸 United States

DELTA

DI: 08033390149860 · Model: 9058.8W.282 · LIMACORPORATE SPA
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DELTA
Primary DI
08033390149860
Version / Model
9058.8W.282
Catalog Number
9058.8W.282
Company Name
LIMACORPORATE SPA
Labeler DUNS
432066322
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-01-05
Public Version
4
Public Version Date
2024-01-08
Public Version Status
Update
Public Device Record Key
8d2d31e4-c522-439a-a22e-9127d68c8c15

Device Description

High Wall Trial Liner Head Dia. 40 mm # 2 EXTRA-LARGE

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
No
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
MBL Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous
LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

GMDN Terms

Code Name
58480 Acetabulum prosthesis trial, prefabricated, reusable

Identifiers

Type ID
Primary 08033390149860

Device Sizes

Type Value Unit Text
Device Size Text, specify Dia. 40 mm # 2 EXTRA-LARGE