FDA UDI In Commercial Distribution 🇺🇸 United States

Dual Tamp

DI: M7391931940000 · Model: 19319-4000 · CAPTIVA SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Dual Tamp
Primary DI
M7391931940000
Version / Model
19319-4000
Company Name
CAPTIVA SPINE, INC.
Labeler DUNS
836975784
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-08-19
Public Version
1
Public Version Date
2022-08-29
Public Version Status
New
Public Device Record Key
fe9520e6-0382-4816-b233-b73bb7970b70

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
32873 Surgical tamp, reusable

Identifiers

Type ID
Primary M7391931940000

Customer Contacts

Phone
561-277-9480