FDA UDI In Commercial Distribution 🇺🇸 United States

Medline Industries, Inc.

DI: 10888277910324 · Model: DYNJCD0193 · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Medline Industries, Inc.
Primary DI
10888277910324
Version / Model
DYNJCD0193
Catalog Number
DYNJCD0193
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-11-07
Public Version
5
Public Version Date
2021-12-22
Public Version Status
Update
Public Device Record Key
48ad4d30-c48b-4ca0-ab8a-a6d87b09f65c

Device Description

CSTM SPINE DRAPE-LF

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
Yes
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
OEQ Angiography/angioplasty kit

GMDN Terms

Code Name
47783 Patient surgical drape, single-use

Identifiers

Type ID
Package 40888277910325
Primary 10888277910324

Customer Contacts