FDA UDI In Commercial Distribution 🇺🇸 United States

mytaMed

DI: B35162068C0 · Model: 6.20.68C · Mytamed, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
mytaMed
Primary DI
B35162068C0
Version / Model
6.20.68C
Catalog Number
6.20.68C
Company Name
Mytamed, Inc.
Labeler DUNS
015903922
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-05-28
Public Version
1
Public Version Date
2020-06-05
Public Version Status
New
Public Device Record Key
d0c11ad7-60cd-4aba-b8bd-dd93742e5c2a

Device Description

Gunter-Gator, Ebonized, 8.0mm Delicate Serrated Jaws

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
Yes
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
62467 Surgical soft-tissue manipulation forceps, alligator, reusable

Identifiers

Type ID
Primary B35162068C0