FDA UDI In Commercial Distribution 🇺🇸 United States

PMT CORPORATION - STEREOTACTIC

DI: 00650551038696 · Model: 2103-102 · PMT CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PMT CORPORATION - STEREOTACTIC
Primary DI
00650551038696
Version / Model
2103-102
Catalog Number
2103-102
Company Name
PMT CORPORATION
Labeler DUNS
039576871
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-11-15
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
2a7a27d9-f1a5-4fe5-a459-f05021c16b58

Device Description

ANCHOR BOLT DRIVER, FOR VERTEK AND BRAINLAB

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
Yes
MRI Safety
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
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
Hydrogen Peroxide

Product Codes

Code Name
HAW Neurological Stereotaxic Instrument

GMDN Terms

Code Name
32568 Neurological stereotactic surgery system

Identifiers

Type ID
Primary 00650551038696

Customer Contacts

Phone
800-626-5463
Phone
800-626-5463

Premarket Submissions

Submission Number Supplement Number
K831329 000