FDA UDI In Commercial Distribution 🇺🇸 United States

EXEL Dermal Curette

DI: 00020221295801 · Model: 29580 · Exel International
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
EXEL Dermal Curette
Primary DI
00020221295801
Version / Model
29580
Catalog Number
29580
Company Name
Exel International
Labeler DUNS
180572216
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-07-15
Public Version
1
Public Version Date
2019-07-23
Public Version Status
New
Public Device Record Key
83368898-e5d7-4af3-9fce-e1c53ba9461c

Device Description

SS, 2.0MM 50PC/BX, 6BX/CS

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
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FZS Curette, Surgical, General Use

GMDN Terms

Code Name
63259 Dermal curette

Identifiers

Type ID
Package 20020221295805
Package 10020221295808
Primary 00020221295801

Customer Contacts

Phone
8009403935