FDA UDI In Commercial Distribution 🇺🇸 United States

TransFasten

DI: M7399851472290 · Model: 98514-7229 · CAPTIVA SPINE, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TransFasten
Primary DI
M7399851472290
Version / Model
98514-7229
Company Name
CAPTIVA SPINE, INC.
Labeler DUNS
836975784
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-08-16
Public Version
1
Public Version Date
2023-08-24
Public Version Status
New
Public Device Record Key
cdc03cb1-0a09-439e-b9b1-78c24afb727c

Device Description

Marking Pin, 229mm, Blunt, SS

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
No
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
LXH Orthopedic Manual Surgical Instrument
KIL Positioner, Socket
FZX Guide, Surgical, Instrument

GMDN Terms

Code Name
62546 Intraoperative orthopaedic bone pin/screw, single-use

Identifiers

Type ID
Primary M7399851472290

Customer Contacts

Phone
561-277-9480

Device Sizes

Type Value Unit Text
Length 229 Millimeter