FDA UDI In Commercial Distribution 🇺🇸 United States

PMI

DI: 00812608021420 · Model: K303 · PROGRESSIVE MEDICAL, INC.
Product Codes
0
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PMI
Primary DI
00812608021420
Version / Model
K303
Catalog Number
K303
Company Name
PROGRESSIVE MEDICAL, INC.
Labeler DUNS
192135242
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-19
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
c2ff99e1-9c67-43a4-85a6-8083e19a9058

Device Description

LACERATION TRAY W/SERRATED FORCEP

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
Yes
Not Made with NRL
No
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

GMDN Terms

Code Name
56303 Suture kit, non-medicated

Identifiers

Type ID
Package 00812608021437
Primary 00812608021420

Customer Contacts

Phone
314-961-5786