Customed
Endotracheal Tube Uncuffed, Size: 5.5MM
9manufacturers in China registered for this device type
18catalogue numbers in this listing
Who Else Makes It
Concentrated in Jiangsu (2), Guangdong (2), Zhejiang (1). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Flexicare Medical (Dongguan) Ltd. | Dongguan | Guangdong | Contract manufacturer | 48 |
| Well Lead Medical Co., Ltd. | Guangzhou | Guangdong | Contract manufacturer | 46 |
| Hangzhou Jinlin Medical Appliances Co., Ltd. | Hangzhou | Zhejiang | Contract manufacturer | 11 |
| Jiangxi Yikang Medical Instrument Group Co., Ltd. | Nanchang | Jiangxi | Contract manufacturer | 2 |
| Jiangsu NEW Pentastar Medical Products Co., Ltd. | Changzhou | Jiangsu | Exporter | 146 |
| Jiangsu Weikang Jiejing Medical Apparatus Co., Ltd. | Shuyang | Jiangsu | Contract manufacturer | 18 |
| Qingdao Traworks Co., Ltd. | Qingdao | Shandong | Exporter | 7 |
| Tianjin Medis Medical Device Co., Ltd. | Tianjin | Tianjin | Contract manufacturer | 5 |
| Chilecom Medical Devices Co Ltd | Xiangtan | Hunan | Manufacturer | 5 |
Record
| Listed by | Customed, Inc., United States |
|---|---|
| FDA product code | BTR |
| Device type | Tube, Tracheal (W/Wo Connector) |
| Device class | Class 2 |
| Regulation | 21 CFR 868.5730 |
| Establishment | Repacker / relabeller, Manufacturer |
| 510(k) | K042683 |
| Record published | 2016-09-23 |
| Record revised | 2020-06-19 (version 4) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Latex | Labelled latex-free |
| Label carries | lot or batch number, expiry date, manufacturing date |
| Storage | Special storage condition: Do not use lubricant with petroleum base.; Special storage condition: Store in clean, cool, and dry place, avoid heat and light. |
| Packaging | 10/box of 10, 10/box 10box/cs of 10, 10/box, 10box/cs of 10, 10/box, 10 box/cs of 10 |
| Sizes | Lumen/inner diameter 2 to 10 mm |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 712057143013 | Lumen/Inner Diameter 8.0 mm | In distribution |
| 712057143006 | Lumen/Inner Diameter 5.5 mm | In distribution |
| 712057143003 | Lumen/Inner Diameter 4.0 mm | In distribution |
| 712057143014 | Lumen/Inner Diameter 8.5 mm | In distribution |
| 712057143011 | Lumen/Inner Diameter 7.0 mm | In distribution |
| 712057143016 | Lumen/Inner Diameter 10.0 mm | In distribution |
| 712057143007 | Lumen/Inner Diameter 5.0 mm | In distribution |
| 712057143001 | Lumen/Inner Diameter 3.0 mm | In distribution |
| 712057143009 | Lumen/Inner Diameter 6.0 mm | In distribution |
| 712057143002 | Lumen/Inner Diameter 3.5 mm | In distribution |
| 712057143008 | Lumen/Inner Diameter 5.5 mm | In distribution |
| 712057143015 | Lumen/Inner Diameter 9.0 mm | In distribution |
| 712057143004 | Lumen/Inner Diameter 4.5 mm | In distribution |
| 712057143012 | Lumen/Inner Diameter 7.5 mm | In distribution |
| 712057142999 | Lumen/Inner Diameter 2.0 mm | In distribution |
| 712057143005 | Lumen/Inner Diameter 5.0 mm | In distribution |
| 712057143000 | Lumen/Inner Diameter 2.5 mm | In distribution |
| 712057143010 | Lumen/Inner Diameter 6.5 mm | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Rusch | Teleflex Medical LLC | 301 |
| Shiley | Covidien LP | 295 |
| Mallinckrodt | Covidien LP | 258 |
| Hudson RCI | Teleflex Medical LLC | 241 |
| Portex | ICU Medical, Inc | 208 |
| Parker Flex-Tip | Salter Labs | 164 |
| Parker | Salter Labs | 157 |
| Curaplex | Bound Tree Medical, LLC | 149 |
| SourceMark | Sourcemark, LLC. | 148 |
| Montgomery® Safe-T-Tube™ | Boston Medical Products, Inc. | 144 |
| Sunmed | SunMed Group Holdings, LLC | 112 |
| Forsure | Forsure Medical Products LLC. | 101 |
Showing 12 of 374. All products under Tube, Tracheal (W/Wo Connector)
Recalls Naming This Product
1 recall names this product by its own identifier, the 510(k) it is cleared under.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity |
|---|---|---|---|---|---|---|
| Well Lead Medical Co., Ltd. | 510(k) number | 2026-07-31 | Not classified | Process control | The 6Fr suction catheter could not pass through the samples smoothly. | 27200 |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.