FDA Device Establishments · JSON-LD · Markdown
FEI 1041732 · Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device for Another Party (Contract Manufacturer) Manufacture Medical Device · Status: Active
| FEI Number | 1041732 |
|---|---|
| Owner / Operator | Attindas (#9099003) |
| Address | 1029 Old Creek Rd, GREENVILLE, NC, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | KME |
| Regulation § (21 CFR) | 880.6060 |
| Proprietary names | ATTENDS DRI-SORB UNDERPAD UFS-230 23X24 20/10; ATTENDS ALL IN ONE ADVANCE PREMIUM UNDERPAD ASB-3036 30X36 12/5; ATTENDS SUPERSORB BARIATRIC UNDERPAD ASBXL EXTRA LARGE 36X51 6/5; ATTENDS DRI-SORB UNDERPAD (HDIS) UFS-230 23X24 20/10; ATTENDS DRI-SORB UNDERPAD (INNO) UFS-236 23X36 15/10; ATTENDS DRI-SORB UNDERPAD UFS-170 17X24 30/10; ATTENDS DRI-SORB ADVANCED UNDERPAD WITH POLYMER UFP-236 23X36 15/10; ATTENDS DRI-SORB UNDERPAD UFS-300 30X30 15/10; ATTENDS SUPERSORB ADVANCE PREMIUM UNDERPAD ASB-300 30X36 12/5; ATTENDS DRI-SORB UNDERPAD UFS-236 23X36 15/10 |
Source: openFDA. Public-domain (CC0).