FDA UDI Not in Commercial Distribution 🇺🇸 United States

PMI

DI: 00812608021048 · Model: PMIIN12 · PROGRESSIVE MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PMI
Primary DI
00812608021048
Version / Model
PMIIN12
Catalog Number
PMIIN12
Company Name
PROGRESSIVE MEDICAL, INC.
Labeler DUNS
192135242
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
2a8906c0-728d-4991-8bca-67801244e72c
Distribution End Date
2016-12-27

Device Description

PMI Pneumoperitoneum Insufflation Needle 12cm

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
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

Product Codes

Code Name
FHO Pneumoperitoneum Needle

GMDN Terms

Code Name
12750 Spring-loaded pneumoperitoneum needle, single-use

Identifiers

Type ID
Package 10812608021045
Primary 00812608021048

Customer Contacts

Phone
314-961-5786