FDA UDI In Commercial Distribution 🇺🇸 United States

SafeView

DI: 00850022178771 · Model: 5801.4602 · Restor3d, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SafeView
Primary DI
00850022178771
Version / Model
5801.4602
Catalog Number
5801.4602
Company Name
Restor3d, Inc.
Labeler DUNS
080819836
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-10-12
Public Version
3
Public Version Date
2023-11-02
Public Version Status
Update
Public Device Record Key
bb4d0a94-6b5e-4e42-8db0-16d29c148ca9

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
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
58752 Arthroscopic access cannula, single-use

Identifiers

Type ID
Primary 00850022178771