FDA UDI In Commercial Distribution 🇺🇸 United States

MEDLINE RENEWAL

DI: 10888277395114 · Model: 005979095RH · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
MEDLINE RENEWAL
Primary DI
10888277395114
Version / Model
005979095RH
Catalog Number
005979095RH
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-01-14
Public Version
1
Public Version Date
2025-01-22
Public Version Status
New
Public Device Record Key
fdc8f04b-864e-4402-a527-e98a6a618e72

Device Description

00-5979-095-29 PATELLA REAMER BLADE WIT

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
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HTO REAMER

GMDN Terms

Code Name
61806 Bone-resection orthopaedic reamer, reprocessed

Identifiers

Type ID
Primary 10888277395114

Customer Contacts