FDA UDI In Commercial Distribution 🇺🇸 United States

PMI

DI: 00812608020270 · Model: PMISG12B4 · PROGRESSIVE MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PMI
Primary DI
00812608020270
Version / Model
PMISG12B4
Catalog Number
PMISG12B4
Company Name
PROGRESSIVE MEDICAL, INC.
Labeler DUNS
192135242
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
5
Public Version Date
2022-06-17
Public Version Status
Update
Public Device Record Key
0cf8979f-ec53-44b2-b72b-1276e78580f5

Device Description

PMI Suture Guide Bariatric Length (12mm - 4 Holes) - Reusable

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
["Moist Heat or Steam Sterilization", "Ethylene Oxide"]

Product Codes

Code Name
FZX Guide, Surgical, Instrument

GMDN Terms

Code Name
60734 Needle guide, reusable

Identifiers

Type ID
Package 10812608020277
Primary 00812608020270

Customer Contacts

Phone
314-961-5786