FDA UDI In Commercial Distribution 🇺🇸 United States

Tranquil-L™

DI: B6788232000 · Model: 823200 · NEXUS SPINE, L.L.C.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Tranquil-L™
Primary DI
B6788232000
Version / Model
823200
Company Name
NEXUS SPINE, L.L.C.
Labeler DUNS
028137605
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-12-17
Public Version
5
Public Version Date
2024-07-12
Public Version Status
Update
Public Device Record Key
7fdc30a4-3f4b-49f4-9d06-9fad7c74757f

Device Description

DLIF Trial 12x22mm, 12 deg

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
No
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
HWT Template

GMDN Terms

Code Name
46479 Surgical implant template, reusable

Identifiers

Type ID
Primary B6788232000
Direct Marking B678823200

Device Sizes

Type Value Unit Text
Width 22 Millimeter
Height 12 Millimeter