FDA UDI In Commercial Distribution 🇺🇸 United States

PLS

DI: 00810086193547 · Model: PLS-845T57 · SINTEA USA, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PLS
Primary DI
00810086193547
Version / Model
PLS-845T57
Company Name
SINTEA USA, LLC
Labeler DUNS
079917057
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-12-04
Public Version
1
Public Version Date
2024-12-12
Public Version Status
New
Public Device Record Key
1f31703f-af34-446e-be87-979e0733a2c6

Device Description

3LOCK- Dual-lead multiaxial cannulated fenestrated screw- l.45mm-ø7mm

Device Characteristics

Single Use
Yes
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
No
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
KWP Appliance, Fixation, Spinal Interlaminal

GMDN Terms

Code Name
65116 Bone-screw internal spinal fixation system rod

Identifiers

Type ID
Primary 00810086193547

Customer Contacts

Phone
3054906850

Premarket Submissions

Submission Number Supplement Number
K140787 000