FDA UDI In Commercial Distribution 🇺🇸 United States

ELMED

DI: 00842180191389 · Model: ST13900GL · ELMED INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
ELMED
Primary DI
00842180191389
Version / Model
ST13900GL
Catalog Number
ST13900GL
Company Name
ELMED INCORPORATED
Labeler DUNS
049290364
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-04-10
Public Version
1
Public Version Date
2024-04-18
Public Version Status
New
Public Device Record Key
17eeec8e-5e0c-4c56-8ffd-d2438c9a560e

Device Description

STAINLESS STEEL CATH GUIDE 653MM X 2MM

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
No
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
MDM Instrument, Manual, Surgical, General Use

GMDN Terms

Code Name
44058 General surgical procedure kit, non-medicated, reusable

Identifiers

Type ID
Primary 00842180191389

Customer Contacts

Phone
224-353-6446