FDA UDI In Commercial Distribution 🇺🇸 United States

NEODERM

DI: 10653405014553 · Model: 740-1000 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
500

Basic Information

Brand Name
NEODERM
Primary DI
10653405014553
Version / Model
740-1000
Catalog Number
740-1000
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
500
Record Status
Published
Publish Date
2020-04-28
Public Version
2
Public Version Date
2024-02-13
Public Version Status
Update
Public Device Record Key
ca9898a0-255b-4f6c-9380-9eb227ac782e

Device Description

NeoDerm Transparent Dressing 2 x 3

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
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MGP Dressing, wound and burn, occlusive

GMDN Terms

Code Name
33963 Peripheral intravenous catheterization support kit

Identifiers

Type ID
Package 20653405014550
Primary 10653405014553
Unit of Use 00653405014556

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K950065 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
10 – 32 Degrees Celsius
Type
Storage Environment Temperature
Temperature Range
50 – 90 Degrees Fahrenheit