FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 20888277418865 · Model: MDTZ1010923AJ · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
12

Basic Information

Brand Name
Medline
Primary DI
20888277418865
Version / Model
MDTZ1010923AJ
Catalog Number
MDTZ1010923AJ
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
12
Record Status
Published
Publish Date
2016-10-14
Public Version
3
Public Version Date
2019-11-08
Public Version Status
Update
Public Device Record Key
12992071-0974-4268-9185-d481ee6d4d80

Device Description

WRAPPER,INSTRUMENT,CEIL,A-S,19PKTS

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
FRG Wrap, sterilization

GMDN Terms

Code Name
40517 Sterilization packaging, reusable

Identifiers

Type ID
Package 30888277418862
Primary 20888277418865
Unit of Use 10888277418868

Customer Contacts