Powerled TM
PWD30 DUAL NAVY SHIP New instal. kit
5manufacturers in China registered for this device type
287catalogue numbers in this listing
3recalls on this code
Who Else Makes It
Concentrated in Guangdong (2), Shandong (1), Jiangxi (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Shenzhen Kaiyan Medical Equipment Co., Ltd. | Shenzhen | Guangdong | Contract manufacturer | 17 |
| Beijing Aeonmed Co., Ltd. | Sanhe | Hebei | Contract manufacturer | 7 |
| Guangdong Kareway Medical Technology Co., Ltd. | Foshan | Guangdong | Manufacturer | 16 |
| Shandong Deman Medical Equipment Group Co., Ltd. | Jining | Shandong | Manufacturer | 11 |
| Nanchang Micare Medical Equipment Co., Ltd. | Nanchang | Jiangxi | Manufacturer | 8 |
Record
| Listed by | Maquet Gmbh, Germany |
|---|---|
| FDA product code | FSY |
| Device type | Light, Surgical, Ceiling Mounted |
| Device class | Class 2 |
| Regulation | 21 CFR 878.4580 |
| Establishment | Specification developer, Repacker / relabeller, Manufacturer |
| 510(k) | K070442 |
| Record published | 2016-09-16 |
| Record revised | 2024-12-11 (version 8) |
Specifications
| MRI safety | MR Unsafe |
|---|---|
| Label carries | manufacturing date, serial number |
| Storage | Handling environment temperature -10 to 60 °C; Storage environment temperature -10 to 60 °C; Handling environment humidity 20 to 75 % RH; Storage environment humidity 20 to 75 % RH; Handling environment atmospheric pressure 50 to 106 KiloPascal; Storage environment atmospheric pressure 50 to 106 KiloPascal |
| Distribution end date | 2020-08-27 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| ARD568424110A | In distribution | |
| ARD267800330A | In distribution | |
| ARD568414110A | In distribution | |
| ARD568474114A | In distribution | |
| ARDPWD259009A | Withdrawn | |
| ARDPWD239002A | Withdrawn | |
| ARDPWD259015A | Withdrawn | |
| ARD568441053A | Withdrawn | |
| ARDROL309009A | Withdrawn | |
| ARD568411513A | Withdrawn | |
| ARDPWD239003A | Withdrawn | |
| ARD568446751A | Withdrawn | |
| ARDPWD209016A | Withdrawn | |
| ARDPWD229031A | Withdrawn | |
| ARD568424753A | Withdrawn | |
| ARD568421253A | Withdrawn | |
| ARD568431253A | Withdrawn | |
| ARD568414755A | Withdrawn | |
| ARDPWD229001A | Withdrawn | |
| ARDPWD229039A | Withdrawn | |
| ARD568410010A | Withdrawn | |
| ARD568420055A | Withdrawn | |
| ARD568425751A | Withdrawn | |
| ARD568421252A | Withdrawn | |
| ARD515062431A | Withdrawn | |
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| ARD568410055A | Withdrawn | |
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| ARD568484114A | Withdrawn | |
| ARD568424512A | Withdrawn | |
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| ARDPWD259016A | Withdrawn | |
| ARD515061131A | Withdrawn | |
| ARDPWD229030A | Withdrawn | |
| ARDPWD229017A | Withdrawn | |
| ARD568431052A | Withdrawn | |
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| ARDPWD229002A | Withdrawn | |
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| ARD568420752A | Withdrawn | |
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| ARDPWD209028A | Withdrawn | |
| ARDPWD259004A | Withdrawn | |
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| ARD568425513A | Withdrawn | |
| ARDPWD229013A | Withdrawn | |
| ARDPWD208008A | Withdrawn | |
| ARDPWD209015A | Withdrawn | |
| ARDPWD229034A | Withdrawn | |
| ARDPWD229006A | Withdrawn | |
| ARD568421251A | Withdrawn | |
| ARDPWD259034A | Withdrawn | |
| ARD568421051A | Withdrawn | |
| ARD568420053A | Withdrawn | |
| ARD568411051A | Withdrawn | |
| ARD515011911A | Withdrawn | |
| ARD568410512A | Withdrawn | |
| ARD568446710A | Withdrawn | |
| ARD568411255A | Withdrawn | |
| ARDROL309030A | Withdrawn | |
| ARDPWD208011A | Withdrawn | |
| ARD568441010A | Withdrawn | |
| ARD568420513A | Withdrawn | |
| ARDPWD229015A | Withdrawn | |
| ARD568441710A | Withdrawn | |
| ARDPWD209011A | Withdrawn | |
| ARDPWD259007A | Withdrawn | |
| ARDPWD229004A | Withdrawn | |
| ARD568446512A | Withdrawn | |
| ARD568425512A | Withdrawn | |
| ARDPWD239018A | Withdrawn | |
| ARD568431252A | Withdrawn | |
| ARDPWD259030A | Withdrawn | |
| ARDPWD229026A | Withdrawn | |
| ARD568425010A | Withdrawn | |
| ARD515012915A | Withdrawn | |
| ARDPWD229047A | Withdrawn | |
| ARDPWD259000A | Withdrawn | |
| ARD568414710A | Withdrawn | |
| ARDPWD208013A | Withdrawn | |
| ARDPWD239010A | Withdrawn | |
| ARDPWD239011A | Withdrawn | |
| ARD568411252A | Withdrawn | |
| ARDPWD209053A | Withdrawn | |
| ARDPWD208017A | Withdrawn | |
| ARD568431110A | Withdrawn | |
| ARD568421210A | Withdrawn | |
| ARD568431751A | Withdrawn | |
| ARDPWD229007A | Withdrawn | |
| ARD568441751A | Withdrawn | |
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| ARD568410052A | Withdrawn | |
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| ARD568441513A | Withdrawn | |
| ARD568431755A | Withdrawn | |
| ARD568431051A | Withdrawn | |
| ARD568411752A | Withdrawn | |
| ARDPWD239015A | Withdrawn | |
| ARDPWD239006A | Withdrawn | |
| ARDPWD239013A | Withdrawn | |
| ARD568421052A | Withdrawn | |
| ARD568425710A | Withdrawn | |
| ARD568431251A | Withdrawn | |
| ARD568420052A | Withdrawn | |
| ARDPWD229014A | Withdrawn | |
| ARDPWD239016A | Withdrawn |
Showing 250 of 287 catalogue numbers.
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| HarmonyAIR | Steris Corporation | 1,344 |
| Volista | Maquet Gmbh | 677 |
| iCE Surgical Light | Amico Clinical Solutions | 599 |
| Devon | Cardinal Health | 70 |
| Light, Surgical, Ceiling Mounted | Maquet Gmbh | 68 |
| Alyon | Steris Corporation | 64 |
| Medical Boom | Amico Clinical Solutions | 56 |
| Standop Volista® | Maquet Gmbh | 50 |
| Amtai | Amtai Medical Equipment, Inc. | 45 |
| Mira Minor Surgery Light | Amico Lights Corporation | 24 |
| MI Product Line | Medical Illumination International, Inc | 20 |
| Kenex | Kenex (Electro-Medical) Ltd. | 18 |
Showing 12 of 191. All products under Light, Surgical, Ceiling Mounted
Recalls Naming This Product
2 recalls name this product by its own identifiers, the 510(k) it is cleared under.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|---|---|
| Getinge Usa Sales Inc | 510(k) number | 2023-11-08 | Class II | Equipment maintenance | A potential for a light system to fall in the operating room. | 236793 units in total | |
| Maquet Cardiovascular Us Sales, Llc | 510(k) number | 2015-05-29 | Class II | Device Design | Maquet Suspension Arms used with PowerLED/X-TEN/Volista Surgical Light Systems may grind at the junction of the suspension arms which can cause paint chips or particles to fall into the surgical field, when the suspension arms are mounted a | 646 units | 2017-04-07 |
Recalls
The FDA has not published a severity grade for these. Volume alone is not a quality signal: a manufacturer that ships more recalls more.
| Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|
| 2009-10-07 | Not classified | Device Design | Several reports have been received regarding one model of spring arm (Acrobat 200 series) in combination with surgical light from various Manufacturers. All incidents pertain to a crack on the front joint of the Acrobat arm. | 54 | 2012-06-04 |
| 2009-10-07 | Not classified | Device Design | Several reports have been received regarding one model of spring arm (Acrobat 200 series) in combination with surgical light from various Manufacturers. All incidents pertain to a crack on the front joint of the Acrobat arm. | 346 | 2012-06-04 |
| 2009-10-07 | Not classified | Device Design | Several reports have been received regarding one model of spring arm (Acrobat 200 series) in combination with surgical light from various Manufacturers. All incidents pertain to a crack on the front joint of the Acrobat arm. | 331 | 2012-06-04 |
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.