FDA UDI In Commercial Distribution 🇺🇸 United States

FIRSTPASS

DI: 00817470000184 · Model: 22-4036 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
FIRSTPASS
Primary DI
00817470000184
Version / Model
22-4036
Catalog Number
22-4036
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-11-13
Public Version
5
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
c3d23d9e-c679-4abe-8849-b025aa2a4a3c

Device Description

FIRSTPASS NEEDLE AND SUTURE CAPTURE, 5 PER BOX

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
NBH ACCESSORIES,ARTHROSCOPIC

GMDN Terms

Code Name
61143 Suturing needle, single-use

Identifiers

Type ID
Package 20817470000188
Primary 00817470000184

Customer Contacts