FDA UDI In Commercial Distribution 🇺🇸 United States

MODIFIED WOODPECKER AVENIR RASP

DI: 00889024580404 · Model: SSI005030 · Zimmer, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MODIFIED WOODPECKER AVENIR RASP
Primary DI
00889024580404
Version / Model
SSI005030
Catalog Number
SSI005030
Company Name
Zimmer, Inc.
Labeler DUNS
056038268
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-02-11
Public Version
1
Public Version Date
2020-02-19
Public Version Status
New
Public Device Record Key
aa65cbf7-f887-4235-a1c0-d4c100ef573e

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
Yes
Has Lot/Batch Number
No
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
HWA Impactor

GMDN Terms

Code Name
58481 Femoral stem prosthesis trial

Identifiers

Type ID
Primary 00889024580404

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify SZ07