FDA UDI In Commercial Distribution 🇺🇸 United States

Combine Pads

DI: 00616784350110 · Model: 3501 · DYNAREX CORPORATION
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Combine Pads
Primary DI
00616784350110
Version / Model
3501
Company Name
DYNAREX CORPORATION
Labeler DUNS
008124539
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-06-21
Public Version
1
Public Version Date
2021-06-29
Public Version Status
New
Public Device Record Key
17f4c850-86e2-4a52-8ef8-d3da8f1e149a

Device Description

Combine Pads 1/Pouch- Sterile, 5"x9"

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FRL Fiber, Medical, Absorbent
NAB Gauze / Sponge,Nonresorbable For External Use

GMDN Terms

Code Name
58805 Absorbent wound compression pad

Identifiers

Type ID
Package 00616784350127
Primary 00616784350110
Package 00616784350134