FDA UDI In Commercial Distribution 🇺🇸 United States

SureCUT

DI: M95550010 · Model: 5001 · SENTREHEART, INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
SureCUT
Primary DI
M95550010
Version / Model
5001
Catalog Number
5001
Company Name
SENTREHEART, INC
Labeler DUNS
068810802
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-17
Public Version
2
Public Version Date
2020-02-06
Public Version Status
Update
Public Device Record Key
b336dc25-a4c8-4d47-b6d3-b6e206de321f

Device Description

A sterile, hand-held surgical instrument designed for cutting sutures using a mechanical action. It typically has a protected scalpel-like blade or a scissors-like cutting end, and a proximal manual actuator. This is a single-use device.

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
Yes
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
FZT Cutter, Surgical

GMDN Terms

Code Name
63487 Suture cutter, single-use

Identifiers

Type ID
Primary M95550010

Customer Contacts

Phone
650-354-1200