FDA UDI In Commercial Distribution 🇺🇸 United States

Combine Pads

DI: 00616784351131 · Model: 3511 · DYNAREX CORPORATION
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
576

Basic Information

Brand Name
Combine Pads
Primary DI
00616784351131
Version / Model
3511
Company Name
DYNAREX CORPORATION
Labeler DUNS
008124539
Distribution Status
In Commercial Distribution
Device Count in Pkg
576
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
b283cfaf-e1f4-43d9-979b-258e1a679a77

Device Description

Combine Pads, Non-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
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 00616784351124
Primary 00616784351131