AccessGUDID - DEVICE: ORACOTE® (10381780000310)

GUDID

Device Identifier (DI) Information

Brand Name: ORACOTE®
Version or Model: #ORACOTE-PKG-10
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: #ORACOTE-PKG-10
Company Name: Integra Lifesciences Corporation

Primary DI Number: 10381780000310
Issuing Agency: GS1
Commercial Distribution End Date: March 31, 2020
Device Count: 10
Labeler D-U-N-S® Number*: 083171244 *Terms of Use

Device Description: SALVIN OraCOTE® Absorbable Collagen Wound Dressing for Dental Surgery, 3/4in x 1 1/2in

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
45023	Collagen wound matrix dressing	A sterile, bioabsorbable, animal-derived collagen protein matrix designed to provide an occlusive/semi-occlusive cover for wound healing (non-oral) and/or a skin template of living cells (fibroblasts) and/or structural proteins to facilitate the infiltration of native skin elements (e.g., fibroblasts, leukocytes, blood vessels) for skin regeneration. The device is used for various types of partial- and full-thickness wounds, draining wounds, sores/ulcers, skin lacerations/abrasions, burns, and/or surgical wounds. It may combine collagen with other compounds or supplemental dressing materials (e.g., alginate); it is supplied in various forms. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LPG	Material, Dressing, Surgical, Polylactic Acid

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
Special Storage Condition, Specify: Avoid excessive heat and humidity

Clinically Relevant Size

[?]

Size Type Text
Device Size Text, specify: 2 cm x 4 cm
Device Size Text, specify: 3/4 in x 1 1/2 in

Device Record Status

Public Device Record Key: f0393dc7-8f04-4c72-8b5a-1b3507885be2
Public Version Date: April 19, 2021
Public Version Number: 8
DI Record Publish Date: September 11, 2014