CORKSCREW MANUFACTURED BY WALDEMAR LINK GMBH & CO. KG

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Request for Information Form	Contact Information
Company Name	WALDEMAR LINK GMBH & CO. KG
Address	BARKHAUSENWEG 10
City, State, Zip	HAMBURG,
Country	GM
FDA Owner/Operator Phone	--
FDA Medical Specialty Code	OR - Orthopedic
FDA Product Code	HWI
FDA Classification Name	CORKSCREW
FDA Device Classification Code	General Controls
FDA Regulation Number	888.4540
FDA Common Generic Name	CORKSCREW
FDA Proprietary Device Name	CORKSCREW
FDA Owner / Operator Number	8010091
FDA Owner / Operator Name	WALDEMAR LINK GMBH & CO. KG
FDA Establishment Registration Number	9610548
FDA Registered Establishment Name	WALDEMAR LINK GMBH & CO. KG
FDA Operation Code(s)
FDA Listing Date
FDA Listing Status Code	Active
Differentiation	N/A
Keywords	N/A
Description	N/A
Brochure	N/A
Product Website	N/A

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1	AESCULAP AG & CO. KG. AM AESCULAP PLATZ TUTTLINGEN, DONAU, D-78532 GM 49-74-6195-1548 / 610-984-9074	CORKSCREW	VARIOUS MODELS
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3	BIOMET, INC. 56 EAST BELL DR. P.O. BOX 587 WARSAW, IN 46581 US 574-267-6639 / 574-372-1742	FEMORAL HEAD REMOVER	FEMORAL HEAD REMOVER
4	DEPUY INTL., LTD. ST. ANTHONY'S RD. LEEDS, LS11 8DT UK 574-267-8143 4906 / 574-371-4906	WROBLEWSKI FEMORAL CEMENT REMOVER	WROBLEWSKI FEMORAL CEMENT REMOVER
5	ZIMMER TRABECULAR METAL TECHNOLOGY 10 POMEROY RD. PARSIPPANY, NJ 07054 US 800-613-6131 / 201-818-1800	ACETABULAR INSERT REMOVER	ACETABULAR INSERT REMOVER
6	ZIMMER, INC. 345 E. MAIN ST. WARSAW, IN 46580 US 800-613-6131 / 574-372-4485	MULTIPLE	CORKSCREWS