FDA UDI In Commercial Distribution 🇺🇸 United States

MEDLINE INDUSTRIES, INC.

DI: 10080196820764 · Model: DYNJ04230 · MEDLINE INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
MEDLINE INDUSTRIES, INC.
Primary DI
10080196820764
Version / Model
DYNJ04230
Catalog Number
DYNJ04230
Company Name
MEDLINE INDUSTRIES, INC.
Labeler DUNS
025460908
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-12-31
Public Version
1
Public Version Date
2021-01-08
Public Version Status
New
Public Device Record Key
cc8c3be0-8191-4e35-999a-182ac0897cf2

Device Description

HOOK,AMNIO,PLASTIC,STERILE

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
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
HHF REMOVER, INTRAUTERINE DEVICE, CONTRACEPTIVE, HOOK-TYPE

GMDN Terms

Code Name
63417 Low-pressure tubing connector, single-use, sterile

Identifiers

Type ID
Package 40080196820765
Primary 10080196820764

Customer Contacts