FDA UDI In Commercial Distribution 🇺🇸 United States

Allacor P

DI: 00850039927355 · Model: 2 cc · Stimlabs LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Allacor P
Primary DI
00850039927355
Version / Model
2 cc
Catalog Number
AP-0020
Company Name
Stimlabs LLC
Labeler DUNS
067529916
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-03-05
Public Version
2
Public Version Date
2025-07-21
Public Version Status
Update
Public Device Record Key
a8c8ad0d-cb10-4f18-9e92-135dec0737e5

Device Description

Allacor P is derived from human umbilical cord extracellular matrix (ECM) and is indicated for the management of a range of acute and chronic wounds. As a resorbable particulate device, Allacor P is lyophilized and packaged in a sterile vial, allowing the device to be rehydrated and applied directly to the wound.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
Yes
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
No
Has Expiration Date
Yes
Has Donation ID
Yes

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KGN Wound Dressing With Animal-Derived Material(S)

GMDN Terms

Code Name
45023 Animal-derived wound matrix dressing

Identifiers

Type ID
Primary 00850039927355

Customer Contacts