FDA UDI In Commercial Distribution 🇺🇸 United States

Dilator Three (threaded)

DI: M73922311007 · Model: 2231-1007 · CAPTIVA SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Dilator Three (threaded)
Primary DI
M73922311007
Version / Model
2231-1007
Company Name
CAPTIVA SPINE, INC.
Labeler DUNS
836975784
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-07-24
Public Version
1
Public Version Date
2022-08-01
Public Version Status
New
Public Device Record Key
d2bd52a8-ba26-47dd-9bbf-191695106284

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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

GMDN Terms

Code Name
11266 Fixed-diameter cervical dilator, reusable

Identifiers

Type ID
Primary M73922311007

Customer Contacts

Phone
561-277-9480