FDA UDI In Commercial Distribution 🇺🇸 United States

Eclipse

DI: M9701500020000 · Model: 1500-02-000 · Medshape, Inc.
Product Codes
1
GMDN Terms
4
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Eclipse
Primary DI
M9701500020000
Version / Model
1500-02-000
Company Name
Medshape, Inc.
Labeler DUNS
601306413
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-19
Public Version
7
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
70470588-04a1-46f5-bba3-09b0fa897984

Device Description

Universal Tenodesis Disposable Procedure Pack

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
KDD Kit, Surgical Instrument, Disposable

GMDN Terms

Code Name
35685 Orthopaedic bone wire
57874 Suturing unit, single-use
45717 Suture knot pusher, single-use
44877 Ligament graft sizer, noninvasive

Identifiers

Type ID
Primary M9701500020000