FDA UDI In Commercial Distribution 🇺🇸 United States

JEDMED

DI: M6335461300 · Model: 54-6130 · JEDMED INSTRUMENT COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
JEDMED
Primary DI
M6335461300
Version / Model
54-6130
Catalog Number
54-6130
Company Name
JEDMED INSTRUMENT COMPANY
Labeler DUNS
092987189
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-01-19
Public Version
1
Public Version Date
2023-01-27
Public Version Status
New
Public Device Record Key
2fa6fe7b-6cbb-48cb-9e2a-c0e570ac886d

Device Description

FORCEPS POST-NASAL HILDYARD 3.5MM

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
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
KAE Forceps, Ent

GMDN Terms

Code Name
11775 Open-surgery biopsy forceps, reusable

Identifiers

Type ID
Primary M6335461300