FDA UDI In Commercial Distribution 🇺🇸 United States

MEDLINE RENEWAL

DI: 10888277390942 · Model: 540031416RH · 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
10888277390942
Version / Model
540031416RH
Catalog Number
540031416RH
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-02-14
Public Version
1
Public Version Date
2025-02-24
Public Version Status
New
Public Device Record Key
c373c35e-19da-4b5a-af66-6894a6bf82f1

Device Description

5400-31-416 CRESCENTIC BLADE 15MM X 30M

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
GFF BUR, SURGICAL, GENERAL & PLASTIC SURGERY

GMDN Terms

Code Name
63598 Surgical saw blade, reciprocating, reprocessed

Identifiers

Type ID
Primary 10888277390942

Customer Contacts