FDA UDI In Commercial Distribution 🇺🇸 United States

CAPTURE™

DI: 10381780242055 · Model: AW1102 · Ascension Orthopedics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
CAPTURE™
Primary DI
10381780242055
Version / Model
AW1102
Catalog Number
AW1102
Company Name
Ascension Orthopedics, Inc.
Labeler DUNS
942377524
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-08-30
Public Version
5
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
34e8c24a-81bb-495c-90bd-501eb8d03d9a
Distribution End Date
2026-12-31

Device Description

CAPTURE™ Cannulated Screw System Smooth K-Wire is used for temporary fixation.

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
HXI PASSER, WIRE, ORTHOPEDIC

GMDN Terms

Code Name
46165 Orthopaedic guidewire, reusable

Identifiers

Type ID
Secondary M269AW11021
Primary 10381780242055

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 3.95 in L x .035 in dia