Udl Laboratories, Inc.
Country not established
- Devices
- 1
What Udl Laboratories, Inc. makes
Udl Laboratories, Inc. manufactures the BIOBRANE® II (Blue Label), a temporary wound dressing designed to protect and promote healing of partial-thickness burns and skin grafts.
The company’s portfolio is regulated under FDA’s Premarket Approval (PMA) process as a Class III device and is listed in the FDA’s PMA registry. The company is based in the United States.
Catalogue
Biobrane (R) Ii Blue Label Product Ref P870069
Regimes: PMA, withdrawn Registry: PMA
Frequently asked questions
How many devices does Udl Laboratories, Inc. have in the registry?
The registry currently lists 1 device for Udl Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Udl Laboratories, Inc.'s devices?
Among its 1 most recently registered device, Udl Laboratories, Inc. has devices listed in FDA PMA (1 device).
What are the newest devices from Udl Laboratories, Inc. in the registry?
The most recently registered devices listed for Udl Laboratories, Inc. include BIOBRANE (R) II BLUE LABEL PRODUCT.