FDA UDI In Commercial Distribution 🇺🇸 United States

Stryker

DI: 00190776137403 · Model: 480148533 · Avalign Technologies, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Stryker
Primary DI
00190776137403
Version / Model
480148533
Company Name
Avalign Technologies, Inc.
Labeler DUNS
792528510
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-08-11
Public Version
3
Public Version Date
2023-07-06
Public Version Status
Update
Public Device Record Key
5a1b0fb3-b3c7-4e33-a19a-6eb91a7eb29d

Device Description

18mm X 25mm X 33mm X 30 degrees Rasp Trial

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
HTR RASP

GMDN Terms

Code Name
35559 Bone file/rasp, manual, reusable

Identifiers

Type ID
Primary 00190776137403

Customer Contacts