FDA UDI In Commercial Distribution 🇺🇸 United States

Tech-Med

DI: 10665973017904 · Model: 4423M · Dukal LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
144

Basic Information

Brand Name
Tech-Med
Primary DI
10665973017904
Version / Model
4423M
Catalog Number
4423M
Company Name
Dukal LLC
Labeler DUNS
791014871
Distribution Status
In Commercial Distribution
Device Count in Pkg
144
Record Status
Published
Publish Date
2022-12-09
Public Version
1
Public Version Date
2022-12-19
Public Version Status
New
Public Device Record Key
8611bd29-53a2-42d9-8f6b-44d38c8375d3

Device Description

Finger Cot, Latex,Non-powdered

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
Yes
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LZB Finger cot

GMDN Terms

Code Name
47172 Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial

Identifiers

Type ID
Package 20665973017901
Primary 10665973017904
Unit of Use 00665973017907

Customer Contacts

Phone
+1(631)656-3800 ext. 172