FDA UDI In Commercial Distribution 🇺🇸 United States

DYNEK

DI: 00848782041992 · Model: GDK8H805 · Surgical Specialties México, S. de R.L. de C.V.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
DYNEK
Primary DI
00848782041992
Version / Model
GDK8H805
Catalog Number
GDK8H805
Company Name
Surgical Specialties México, S. de R.L. de C.V.
Labeler DUNS
812762226
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-10-22
Public Version
3
Public Version Date
2023-06-02
Public Version Status
Update
Public Device Record Key
48e17502-fccc-4b0f-b071-58c6fa9258b1

Device Description

2xDRS-8.0-230 USP 8-0 Polypropylene blue 75 cm. sterile VA8.1

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
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
No
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
GAW Suture, nonabsorbable, synthetic, polypropylene

GMDN Terms

Code Name
13909 Polyolefin/fluoropolymer suture, monofilament

Identifiers

Type ID
Package 10848782041999
Primary 00848782041992

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K131224 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 8-0 USP