FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 08800043934445 · Model: 1523-5200 · TDM Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
N/A
Primary DI
08800043934445
Version / Model
1523-5200
Catalog Number
1523-5200
Company Name
TDM Co., Ltd.
Labeler DUNS
557801921
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-09-16
Public Version
2
Public Version Date
2024-08-08
Public Version Status
Update
Public Device Record Key
e8bd0cda-c36c-49b1-a159-e62459aabcf9

Device Description

Pine Pre-bent Rod (Sharp Tip) Ø 5.5 x 200 mm

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
NKB Thoracolumbosacral Pedicle Screw System

GMDN Terms

Code Name
65116 Bone-screw internal spinal fixation system rod

Identifiers

Type ID
Primary 08800043934445

Premarket Submissions

Submission Number Supplement Number
K220285 000

Device Sizes

Type Value Unit Text
Length 200 Millimeter