FDA UDI In Commercial Distribution 🇺🇸 United States

PMT® CORPORATION

DI: 00650551098409 · Model: 2105-5 · PMT CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PMT® CORPORATION
Primary DI
00650551098409
Version / Model
2105-5
Catalog Number
2105-5
Company Name
PMT CORPORATION
Labeler DUNS
039576871
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-01-28
Public Version
3
Public Version Date
2024-02-05
Public Version Status
Update
Public Device Record Key
1b0ab09c-982d-432e-b43c-5d044354a454

Device Description

IN-LINE TUNNELING NEEDLE

Device Characteristics

Single Use
Yes
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
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HAO Instrument, Surgical, Non-Powered

GMDN Terms

Code Name
46801 Subcutaneous tunneller, single-use

Identifiers

Type ID
Primary 00650551098409

Customer Contacts

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

Device Sizes

Type Value Unit Text
Needle Gauge 13 Gauge