FDA UDI In Commercial Distribution 🇺🇸 United States

HU-FRIEDY

DI: 10889950019686 · Model: PMP7002 · HU-FRIEDY MFG. CO., LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HU-FRIEDY
Primary DI
10889950019686
Version / Model
PMP7002
Catalog Number
PMP7002
Company Name
HU-FRIEDY MFG. CO., LLC
Labeler DUNS
005085972
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-08-14
Public Version
1
Public Version Date
2020-08-24
Public Version Status
New
Public Device Record Key
12912f31-650b-4045-91de-8b57445c1e01

Device Description

Modified PMPI Membrane Placement Inst.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
No
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
MDM INSTRUMENT, MANUAL, SURGICAL, GENERAL USE

GMDN Terms

Code Name
55847 Dental implant system

Identifiers

Type ID
Primary 10889950019686

Customer Contacts