NNWClass I
Bag, Urine Collection, Leg, For External Use, Non-Sterile
21 CFR 876.5250 / Gastroenterology, Urology
NNW is the FDA product code for Bag, Urine Collection, Leg, For External Use, Non-Sterile, a class I device type, regulated under 21 CFR 876.5250. FDA's definition for this code reads: "Urine collector and accessories; see product code FAQ". As of , FDA records hold no 510(k) clearances under this code and 2 recalls.
Classification record
- Product code
- NNW
- Device name
- Bag, Urine Collection, Leg, For External Use, Non-Sterile
- FDA definition
- Urine collector and accessories; see product code FAQ.
- Regulation
- 21 CFR 876.5250
- Device class
- Class I
- Review panel
- Gastroenterology, Urology
- Submission type
- 510(k) exempt
- Implant
- No
- Life sustaining or supporting
- No
- GMP exempt
- Yes
- Third party review eligible
- No
- Ingested clearances
- 0
- Ingested recalls
- 2
Companies listing this code with FDA
Companies whose registered establishments list this code- Acosta Medical Group Inc.
- Alimed, LLC
- Alltrista Plastics LLC
- Angiplast Pvt. Ltd.
- Anhui Ares Medical Technology Co.,Ltd.
- Anhui Easyway Medical Supplies Co., Ltd
- Anhui Medpurest Medical Technology Co.,Ltd
- Anqing Kangmingna Packaging Co.,Ltd
- Ansell Healthcare Products LLC
- Ansell Sandel Medical Solutions LLC
- Atlas Medical Products LLC
- Beauxregard Industries
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
