FDA UDI In Commercial Distribution 🇺🇸 United States

Kirwan

DI: 00841019107843 · Model: 50-1003 · KIRWAN SURGICAL PRODUCTS LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Kirwan
Primary DI
00841019107843
Version / Model
50-1003
Company Name
KIRWAN SURGICAL PRODUCTS LLC
Labeler DUNS
046355210
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-08
Public Version
5
Public Version Date
2019-08-21
Public Version Status
Update
Public Device Record Key
b1ac9680-05c7-49fb-b009-905c0db37bcf

Device Description

Bankart Shoulder Repair Instrument 7 3/4" (19.7cm) Glenoid Reaming Forceps

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HAO Instrument, Surgical, Non-Powered

GMDN Terms

Code Name
46751 Bone holding forceps

Identifiers

Type ID
Primary 00841019107843

Customer Contacts

Phone
781-834-9500
Phone
781-834-9500

Device Sizes

Type Value Unit Text
Length 7.75 Inch