FDA UDI In Commercial Distribution 🇺🇸 United States

SafeGuard®

DI: 10381780280736 · Model: 080003 · Ascension Orthopedics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
SafeGuard®
Primary DI
10381780280736
Version / Model
080003
Catalog Number
080003
Company Name
Ascension Orthopedics, Inc.
Labeler DUNS
942377524
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-04-13
Public Version
5
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
080c9a6d-3d1c-4013-9705-72430ff5b32b
Distribution End Date
2026-12-31

Device Description

SafeGuard CARPAL TUNNEL KNIFE 1 PIECE

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
Yes
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
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Secondary M2480800031
Primary 10381780280736

Customer Contacts