FDA UDI In Commercial Distribution 🇺🇸 United States

AG Foam Kit Medium

DI: 00849405022121 · Model: AG-MFOAM2 · GENADYNE BIOTECHNOLOGIES INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
AG Foam Kit Medium
Primary DI
00849405022121
Version / Model
AG-MFOAM2
Catalog Number
AG-MFOAM2
Company Name
GENADYNE BIOTECHNOLOGIES INC.
Labeler DUNS
006616130
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-01-21
Public Version
1
Public Version Date
2025-01-29
Public Version Status
New
Public Device Record Key
c41cb5a6-dc1a-4bc0-be62-859992512898

Device Description

XLR8 PU Foam with AG Kit, Medium

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
Yes
MRI Safety
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OMP Negative Pressure Wound Therapy Powered Suction Pump

GMDN Terms

Code Name
47407 Negative-pressure wound therapy system foam dressing, antimicrobial

Identifiers

Type ID
Primary 00849405022121

Premarket Submissions

Submission Number Supplement Number
K082676 000