FDA UDI In Commercial Distribution 🇺🇸 United States

BUDDE®

DI: 10381780355151 · Model: S438A1053 · INTEGRA LIFESCIENCES CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
BUDDE®
Primary DI
10381780355151
Version / Model
S438A1053
Company Name
INTEGRA LIFESCIENCES CORPORATION
Labeler DUNS
963856096
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-29
Public Version
4
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
7d680b67-df09-4e23-81ba-2fde1e6cbbee

Device Description

BUDDE® Drawbar

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
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
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
GZT RETRACTOR, SELF-RETAINING, FOR NEUROSURGERY

GMDN Terms

Code Name
62772 Neurosurgical retraction system, brain

Identifiers

Type ID
Secondary M268S438A10531
Primary 10381780355151

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K830332 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 9.5" Length x 5.5" Width x 0.25" Height