FDA UDI In Commercial Distribution 🇺🇸 United States

SUTUMED

DI: 07757093684282 · Model: SDPP001MC250 · Unilene S.A.C.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
SUTUMED
Primary DI
07757093684282
Version / Model
SDPP001MC250
Company Name
Unilene S.A.C.
Labeler DUNS
934900072
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-01-06
Public Version
2
Public Version Date
2023-06-02
Public Version Status
Update
Public Device Record Key
74b61608-c35e-4b8a-a2b1-cd71cbd0c3bb

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
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
GAW Suture, Nonabsorbable, Synthetic, Polypropylene

GMDN Terms

Code Name
13909 Polyolefin/fluoropolymer suture, monofilament

Identifiers

Type ID
Package 07757093684336
Primary 07757093684282

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K123034 000