FDA UDI In Commercial Distribution 🇺🇸 United States

ACL

DI: 00841132124277 · Model: 01-1008-2530 · ORTHOPEDIATRICS CORP.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ACL
Primary DI
00841132124277
Version / Model
01-1008-2530
Catalog Number
01-1008-2530
Company Name
ORTHOPEDIATRICS CORP.
Labeler DUNS
796416191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-07-06
Public Version
1
Public Version Date
2021-07-14
Public Version Status
New
Public Device Record Key
4b4c536c-07c8-43c9-afcf-c431b689994c

Device Description

2.5MM X 300MM GUIDE WIRE, SMOOTH, COCR

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
Yes
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
FZH Apparatus, air handling, room

GMDN Terms

Code Name
44054 Orthopaedic surgical procedure kit, non-medicated, reusable

Identifiers

Type ID
Primary 00841132124277

Customer Contacts