FDA UDI In Commercial Distribution 🇺🇸 United States

MEDLINE

DI: 10197344695362 · Model: GEMTITAN48TC · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
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
MEDLINE
Primary DI
10197344695362
Version / Model
GEMTITAN48TC
Catalog Number
GEMTITAN48TC
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-09-26
Public Version
1
Public Version Date
2024-10-04
Public Version Status
New
Public Device Record Key
b84e35e0-bf39-4a69-8103-2482a27e5622

Device Description

WRAP,BONDED,2-TONE,48X48,TITAN

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
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
No

Product Codes

Code Name
FRG Wrap, sterilization

GMDN Terms

Code Name
13735 Sterilization packaging, single-use

Identifiers

Type ID
Package 20197344695369
Primary 10197344695362
Package 30197344695366

Customer Contacts