FDA UDI In Commercial Distribution 🇺🇸 United States

16'' DLX POST-OP KNEE IMMOB

DI: 00609271200159 · Model: 462-0012-40 · DARCO INTERNATIONAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
16'' DLX POST-OP KNEE IMMOB
Primary DI
00609271200159
Version / Model
462-0012-40
Catalog Number
462-0012-40
Company Name
DARCO INTERNATIONAL, INC.
Labeler DUNS
184231298
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-02-08
Public Version
1
Public Version Date
2023-02-16
Public Version Status
New
Public Device Record Key
ddb3c0f4-577b-4feb-bd2c-934d8d8dc619

Device Description

Medium

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
Yes
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
No

Product Codes

Code Name
ITQ JOINT, KNEE, EXTERNAL BRACE

GMDN Terms

Code Name
12099 Knee immobilizer

Identifiers

Type ID
Package 10609271200156
Primary 00609271200159
Package 20609271200153