FDA UDI Not in Commercial Distribution 🇺🇸 United States

Integra® Spider™ Limted Wrist Fusion System

DI: 10381780280798 · Model: 075022 · Ascension Orthopedics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Integra® Spider™ Limted Wrist Fusion System
Primary DI
10381780280798
Version / Model
075022
Catalog Number
075022
Company Name
Ascension Orthopedics, Inc.
Labeler DUNS
942377524
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-04-13
Public Version
8
Public Version Date
2023-05-02
Public Version Status
Update
Public Device Record Key
834e18ec-d465-42f2-9be7-e9c5e226cde8
Distribution End Date
2023-03-31

Device Description

STERILIZATION CASE LID

Device Characteristics

Single Use
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
FSM TRAY, SURGICAL, INSTRUMENT

GMDN Terms

Code Name
12143 Instrument tray, reusable

Identifiers

Type ID
Secondary M2480750221
Primary 10381780280798

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 1.01" Height