FDA UDI In Commercial Distribution 🇺🇸 United States

DISTRACTION, INTERNAL

DI: 00888118129192 · Model: 51-402-72-09 · KLS-Martin L.P.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DISTRACTION, INTERNAL
Primary DI
00888118129192
Version / Model
51-402-72-09
Company Name
KLS-Martin L.P.
Labeler DUNS
826499238
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-12-22
Public Version
1
Public Version Date
2020-12-30
Public Version Status
New
Public Device Record Key
11a9943d-78fa-4c2a-abb6-9ae52c69c306

Device Description

PLATE, MODULAR, CRANIAL, SLIDING, 3 MM HOOKS, 1.5-1.8 MM SCREW, CP TITANIUM

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
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
MQN EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR

GMDN Terms

Code Name
47635 Implantable craniofacial bone distractor

Identifiers

Type ID
Primary 00888118129192

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 8 HOLE