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Auckland Medical Polymer (Tianjin) Co., Ltd

Tianjin, CN

Auckland Medical Polymer (Tianjin) Co., Ltd appears in FDA device records in Tianjin, CN. FDA records list one 510(k) clearance, no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.

FDA records held for this company

510(k) clearances
1
PMA records
0
Recall records
0
Registered establishments
1

510(k) clearance history

FDA records hold 1 510(k) clearance for Auckland Medical Polymer (Tianjin) Co., Ltd in 2020.

Clearances by year, as a table
510(k) clearance decisions for Auckland Medical Polymer (Tianjin) Co., Ltd, by decision year
YearClearances
20201
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K183148OKLand Patient Return Electrode PadGEISubstantially Equivalent

Registered establishments

FDA registered establishments for Auckland Medical Polymer (Tianjin) Co., Ltd, with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
30115590893011559089Auckland Medical Polymer (Tianjin) Co., LtdBldg D5-2 XEDA International Industrial Park, Tianjin 300385 CN2026

Registration numbers link to the FDA registration and listing record for that establishment.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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What MDM checks, and what it does not

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Data as of , FDA export datePage updated Source: openFDA, public domain