FDA UDI In Commercial Distribution 🇺🇸 United States

ELMED

DI: 00842180163652 · Model: 23-220 · ELMED INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ELMED
Primary DI
00842180163652
Version / Model
23-220
Catalog Number
23-220
Company Name
ELMED INCORPORATED
Labeler DUNS
049290364
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-04-10
Public Version
1
Public Version Date
2023-04-18
Public Version Status
New
Public Device Record Key
33ef7002-169f-494c-8522-077b6c1c79a8

Device Description

3.2MM 10"DIA., SWITCHING STICK, BLUNT END & BLUNT CONE TIP

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
Yes
Has Lot/Batch Number
Yes
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
NBH Accessories, Arthroscopic

GMDN Terms

Code Name
44091 Arthroscopic surgical procedure kit, non-medicated, reusable

Identifiers

Type ID
Primary 00842180163652

Customer Contacts

Phone
224-353-6446