FDA UDI In Commercial Distribution 🇺🇸 United States

SafePath

DI: 00861298002622 · Model: 1F002 · Safepath Medical, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SafePath
Primary DI
00861298002622
Version / Model
1F002
Company Name
Safepath Medical, Inc.
Labeler DUNS
877189584
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-01-28
Public Version
1
Public Version Date
2022-02-07
Public Version Status
New
Public Device Record Key
4dee76fc-d53d-4841-b7a6-426d0fed7f24

Device Description

One pouched device, 1F002

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
Yes
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GAP Suture, Nonabsorbable, Silk

GMDN Terms

Code Name
13910 Silk suture

Identifiers

Type ID
Primary 00861298002622