How to Use
To apply PuraPly AM, follow these simple steps1:
  1. Prepare wound to ensure it is free of debris and necrotic tissue
  2. Cut the dry sheet to the appropriate size and place in contact with wound bed
  3. Hydrate with sterile saline as needed
  4. Apply appropriate fixation and secondary dressings
  5. Assess weekly for reapplication
  1. PuraPly Antimicrobial [package insert]. Canton, MA: Organogenesis, Inc; 2015.
Storage & Sizes

PuraPly AM is supplied in an individually sealed dry sheet and packaged in a sterile, sealed single pouch. PuraPly AM offers convenient room temperature storage and comes in the following sizes to manage a wide variety of wound types.1,2*

Product CodeProduct Description/SizeUDI Number
PURAPLYAM-COM 1.6 DISC1.6cm Disc00618474000190
PURAPLYAM-COM 2X22cm x 2cm00618474000084
PURAPLYAM-COM 2.05X3.052.05cm x 3.05cm00618474000329
PURAPLYAM-COM 2X42cm x 4cm00618474000091
PURAPLYAM-COM 3.02x3.023.02cm x 3.02cm00618474000299
PURAPLYAM-COM 3.76X3.763.76cm x 3.76cm00618474000305
PURAPLYAM-COM 5X55cm x 5cm00618474000107
PURAPLYAM-COM 6X96cm x 9cm00618474000114
PURAPLYAM-COM 8X168cm x 16cm00618474000121
* Do not freeze or expose PuraPly AM to excessive heat.

PuraPly Antimicrobial consists of a native ECM coated with 0.1% polyhexamethylenebiguanide hydrochloride (PHMB) intended for the management of wounds.

  • This device is not intended for use in third-degree burns
  • This device is derived from a porcine source and should not be used in patients with known sensitivity to porcine material
  • Do not use on individuals with a known sensitivity to polyhexamethylene biguanide hydrochloride (PHMB)

Do not resterilize. The device is intended for single-patient use only. Do not reuse. Discard all open and unused portions. PuraPly AM is sterile if the package is dry, unopened, and undamaged. Do not use if the package seal is broken. PuraPly AM must be used prior to the expiration date. Discard PuraPly AM if mishandling has caused possible damage or contamination. PuraPly AM should not be applied until excessive exudate, bleeding, acute infection, and significant swelling are controlled.

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