FDA UDI In Commercial Distribution 🇺🇸 United States

AVALIGN

DI: 00850011214183 · Model: PMI-LK75-2974/09 · PROGRESSIVE MEDICAL INSTRUMENTATION INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AVALIGN
Primary DI
00850011214183
Version / Model
PMI-LK75-2974/09
Catalog Number
PMI-LK75-2974/09
Company Name
PROGRESSIVE MEDICAL INSTRUMENTATION INC
Labeler DUNS
131054074
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-09-06
Public Version
1
Public Version Date
2019-09-16
Public Version Status
New
Public Device Record Key
2dd4f182-cde1-48ba-b81e-4c8fc59ede7c

Device Description

IVD RONG STR 5X10MM 11.75"

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HAE Rongeur, Manual

GMDN Terms

Code Name
32853 Orthopaedic joint/limb rongeur

Identifiers

Type ID
Primary 00850011214183

Customer Contacts

Phone
5022671100