FDA UDI In Commercial Distribution 🇺🇸 United States

TIMX

DI: 10705034000589 · Model: 202582 · Medos International Sàrl
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TIMX
Primary DI
10705034000589
Version / Model
202582
Catalog Number
202582
Company Name
Medos International Sàrl
Labeler DUNS
482661753
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-31
Public Version
3
Public Version Date
2018-12-07
Public Version Status
Update
Public Device Record Key
2077492e-3ffe-4627-ac2e-4e4d50d5fdf3

Device Description

TIMX LOW BACK SYSTEM DEPTH GAUGE 0-60mm Plus or Minus 21 Percent

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
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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HTJ GAUGE, DEPTH

GMDN Terms

Code Name
32845 Surgical depth gauge, reusable

Identifiers

Type ID
Primary 10705034000589

Customer Contacts