FDA UDI In Commercial Distribution 🇺🇸 United States

PMI

DI: 00812608022328 · Model: PMICC512S · PROGRESSIVE MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
PMI
Primary DI
00812608022328
Version / Model
PMICC512S
Company Name
PROGRESSIVE MEDICAL, INC.
Labeler DUNS
192135242
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-11-12
Public Version
1
Public Version Date
2024-11-20
Public Version Status
New
Public Device Record Key
8ef2b571-d135-4e9a-9a73-61e6da01c8b9

Device Description

PMI Disposable Classic Closure Kit (4 piece) (1) PMI Disposable Classic Closure Device, (1) PMI Disposable 10/12mm Suture Guide, (1) PMI Disposable 5/8mm Suture Guide, (1) Trocar Cleaning Swab Pack

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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KDD Kit, Surgical Instrument, Disposable

GMDN Terms

Code Name
57874 Suturing unit, single-use

Identifiers

Type ID
Package 00812608022335
Primary 00812608022328