FDA UDI In Commercial Distribution 🇺🇸 United States

FOOTPRINT

DI: 03596010650498 · Model: 72202986 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FOOTPRINT
Primary DI
03596010650498
Version / Model
72202986
Catalog Number
72202986
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-29
Public Version
6
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
074c8f4b-da98-46ba-bc1b-d2ee91d51973

Device Description

3.8 MM STRAIGHT AWL-DISPOSABLE

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
15275 Bone awl, reusable

Identifiers

Type ID
Primary 03596010650498

Customer Contacts