FDA UDI In Commercial Distribution 🇺🇸 United States

Medline

DI: 10888277690073 · Model: MPP100660SS · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Medline
Primary DI
10888277690073
Version / Model
MPP100660SS
Catalog Number
MPP100660SS
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-12-23
Public Version
1
Public Version Date
2020-12-31
Public Version Status
New
Public Device Record Key
551ba035-24f0-454f-aec9-86222e153bb1

Device Description

POUCH TYVEK 7.5X13 SELF STERRAD

Device Characteristics

Single Use
Yes
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FRG Wrap, sterilization

GMDN Terms

Code Name
13735 Sterilization packaging, single-use

Identifiers

Type ID
Package 30888277690077
Primary 10888277690073
Package 20888277690070

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K123162 000