FDA UDI In Commercial Distribution 🇺🇸 United States

Sil-serter™

DI: 00643169705920 · Model: MMT-385 · MEDTRONIC MINIMED, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Sil-serter™
Primary DI
00643169705920
Version / Model
MMT-385
Company Name
MEDTRONIC MINIMED, INC.
Labeler DUNS
849626338
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-09-17
Public Version
1
Public Version Date
2022-09-26
Public Version Status
New
Public Device Record Key
ec286c58-15d3-46d2-bcf2-0ce29e51058a

Device Description

LANCET DEVICE MMT-385 SILSRTR EA 21L SMC

Device Characteristics

Single Use
No
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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KZH INTRODUCER, SYRINGE NEEDLE

GMDN Terms

Code Name
45449 Injector reset device

Identifiers

Type ID
Primary 00643169705920

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K010377 000