FDA UDI In Commercial Distribution 🇺🇸 United States

ORCA Foam

DI: 00860008294333 · Model: Size 4 · Orca Products, LLC
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
20

Basic Information

Brand Name
ORCA Foam
Primary DI
00860008294333
Version / Model
Size 4
Company Name
Orca Products, LLC
Labeler DUNS
117716283
Distribution Status
In Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2023-09-15
Public Version
2
Public Version Date
2023-12-20
Public Version Status
Update
Public Device Record Key
2d48b730-fd8b-48fb-8fce-5c22bba812ce

Device Description

AbsorbaleGelatin Sponge

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
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
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
LYA Splint, Intranasal Septal
KHJ Polymer, Ent Synthetic-Polyamide (Mesh Or Foil Material)

GMDN Terms

Code Name
48170 Gelatin haemostatic agent

Identifiers

Type ID
Unit of Use 00860008294302
Primary 00860008294333

Customer Contacts

Phone
334-803-2370