FDA UDI In Commercial Distribution 🇺🇸 United States

ELMED

DI: 00842180152045 · Model: 52103-37I · ELMED INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ELMED
Primary DI
00842180152045
Version / Model
52103-37I
Catalog Number
52103-37I
Company Name
ELMED INCORPORATED
Labeler DUNS
049290364
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-23
Public Version
1
Public Version Date
2023-01-02
Public Version Status
New
Public Device Record Key
28c7381e-6fb6-4b54-8133-0adb932d15e9

Device Description

INSERT ONLY, 10MM DIA., 36CM BIOPSY SPOON FORCEPS, SINGLE ACTION

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
No
Has Serial Number
No
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
GCJ Laparoscope, General & Plastic Surgery

GMDN Terms

Code Name
32043 Laparoscopic surgical procedure kit, non-medicated, reusable

Identifiers

Type ID
Primary 00842180152045

Customer Contacts

Phone
224-353-6446

Premarket Submissions

Submission Number Supplement Number
K181173 000