FDA UDI In Commercial Distribution 🇺🇸 United States

90210 Single Use #10 Safety Scalpel

DI: 00787551012101 · Model: 90210 · XODUS MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
90210 Single Use #10 Safety Scalpel
Primary DI
00787551012101
Version / Model
90210
Catalog Number
90210
Company Name
XODUS MEDICAL, INC.
Labeler DUNS
868042664
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-08
Public Version
1
Public Version Date
2022-12-16
Public Version Status
New
Public Device Record Key
6343edd8-6b8f-415c-a6f2-df6a6d56d44e

Device Description

90210 Single Use #10 Safety Scalpel

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Radiation Sterilization

Product Codes

Code Name
GES BLADE, SCALPEL

GMDN Terms

Code Name
47569 Scalpel, single-use

Identifiers

Type ID
Package 10787551012108
Primary 00787551012101
Package 20787551012105

Customer Contacts