FDA UDI In Commercial Distribution 🇺🇸 United States

Affixus®

DI: 00887868582271 · Model: 211300400 · Zimmer, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Affixus®
Primary DI
00887868582271
Version / Model
211300400
Catalog Number
211300400
Company Name
Zimmer, Inc.
Labeler DUNS
056038268
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-10-17
Public Version
1
Public Version Date
2024-10-25
Public Version Status
New
Public Device Record Key
e6b43d00-55bf-4326-9a8b-2f370eeb3037

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
HTO REAMER

GMDN Terms

Code Name
35297 Medullary canal orthopaedic reamer, flexible

Identifiers

Type ID
Primary 00887868582271

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Length 400 mm