FDA UDI In Commercial Distribution 🇺🇸 United States

Combine Pads

DI: 00616784351339 · Model: 3513 · DYNAREX CORPORATION
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
432

Basic Information

Brand Name
Combine Pads
Primary DI
00616784351339
Version / Model
3513
Company Name
DYNAREX CORPORATION
Labeler DUNS
008124539
Distribution Status
In Commercial Distribution
Device Count in Pkg
432
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
d18b920e-2a75-438c-bdf7-0b59c3d3cc81

Device Description

Combine Pads- Non-Sterile 8"x10"

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
No
Sterilization Prior Use
No

Product Codes

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

GMDN Terms

Code Name
58805 Absorbent wound compression pad

Identifiers

Type ID
Unit of Use 00616784351322
Primary 00616784351339