FDA UDI In Commercial Distribution 🇺🇸 United States

Suture USP 0

DI: 17350154050551 · Model: BOM 1055S rev 05 Suture PDO USP 0 - Sterilized · Suturion AB
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
12

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
Suture USP 0
Primary DI
17350154050551
Version / Model
BOM 1055S rev 05 Suture PDO USP 0 - Sterilized
Company Name
Suturion AB
Labeler DUNS
353236163
Distribution Status
In Commercial Distribution
Device Count in Pkg
12
Record Status
Published
Publish Date
2025-12-15
Public Version
1
Public Version Date
2025-12-23
Public Version Status
New
Public Device Record Key
9e11e4e1-5a5b-43de-ae5f-3337c70476d9

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
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
NEW Suture, Surgical, Absorbable, Polydioxanone

GMDN Terms

Code Name
16584 Polyester suture, bioabsorbable, monofilament, non-antimicrobial

Identifiers

Type ID
Primary 17350154050551
Unit of Use 07350154050554

Premarket Submissions

Submission Number Supplement Number
K250977 000