FDA UDI In Commercial Distribution 🇺🇸 United States

Vacurect

DI: 00861753000200 · Model: Custom 1002 · MAINSPRING MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Vacurect
Primary DI
00861753000200
Version / Model
Custom 1002
Company Name
MAINSPRING MEDICAL, LLC
Labeler DUNS
133686100
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-09
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
8afe96ce-45f8-4231-95b4-73ed2a493953

Device Description

Vacurect vacuum erection device with 5 tension systems, 2 oz personal lubricant, storage pouch, user's guide, and 1 year warranty.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LKY Device, External Penile Rigidity

GMDN Terms

Code Name
17744 Penile vacuum device

Identifiers

Type ID
Primary 00861753000200

Customer Contacts

Phone
7064264145