FDA UDI In Commercial Distribution 🇺🇸 United States

SunMed

DI: 10889483007372 · Model: 9-3018-02 · SUNMED, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
SunMed
Primary DI
10889483007372
Version / Model
9-3018-02
Catalog Number
9-3018-02
Company Name
SUNMED, LLC
Labeler DUNS
069009268
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-03-12
Public Version
1
Public Version Date
2024-03-20
Public Version Status
New
Public Device Record Key
90b7498e-6aad-4792-bcee-6c19fd655375

Device Description

MAGILL STEEL CHILD FORCEPS

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
Yes
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
No

Product Codes

Code Name
KAE FORCEPS, ENT

GMDN Terms

Code Name
65449 ENT foreign body extraction forceps

Identifiers

Type ID
Primary 10889483007372

Customer Contacts