FDA UDI In Commercial Distribution 🇺🇸 United States

DFX Tensile Tape

DI: 10854629006830 · Model: DFX0033S · DUNAMIS MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
DFX Tensile Tape
Primary DI
10854629006830
Version / Model
DFX0033S
Catalog Number
DFX0033S
Company Name
DUNAMIS MEDICAL, LLC
Labeler DUNS
079471560
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-08-11
Public Version
1
Public Version Date
2023-08-21
Public Version Status
New
Public Device Record Key
98d99957-a94c-4de2-9000-8a38099d6770

Device Description

2mm White 39" Fiber Connect Tape

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
No
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
GAT Suture, Nonabsorbable, Synthetic, Polyethylene

GMDN Terms

Code Name
13907 Polyolefin/fluoropolymer suture, multifilament

Identifiers

Type ID
Primary 10854629006830

Customer Contacts

Phone
731-217-2533

Premarket Submissions

Submission Number Supplement Number
K153746 000