FDA UDI In Commercial Distribution 🇺🇸 United States

STOPLOSS® JONES TUBE INTRODUCER SET

DI: 13700773730817 · Model: S1.7500 · FCI S A S FCI 20 22
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
STOPLOSS® JONES TUBE INTRODUCER SET
Primary DI
13700773730817
Version / Model
S1.7500
Company Name
FCI S A S FCI 20 22
Labeler DUNS
763408366
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-04-20
Public Version
1
Public Version Date
2026-04-28
Public Version Status
New
Public Device Record Key
5e450539-4746-4171-bd87-5a6f046977a6

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
OKS Lacrimal Stents And Intubation Sets

GMDN Terms

Code Name
45150 Ophthalmic surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Primary 13700773730817