Primary Device ID | 50885403184480 |
NIH Device Record Key | d66d62a1-c0c0-4a13-90ae-e98345086ed3 |
Commercial Distribution Discontinuation | 2023-09-30 |
Commercial Distribution Status | Not in Commercial Distribution |
Version Model Number | 4469A |
Catalog Number | 4469A |
Company DUNS | 832696038 |
Company Name | CAREFUSION 2200, INC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | true |
Phone | +1(800)523-0502 |
Customer_Support@BD.com | |
Phone | +1(800)523-0502 |
Customer_Support@BD.com | |
Phone | +1(800)523-0502 |
Customer_Support@BD.com | |
Phone | +1(800)523-0502 |
Customer_Support@BD.com | |
Phone | +1(800)523-0502 |
Customer_Support@BD.com | |
Phone | +1(800)523-0502 |
Customer_Support@BD.com | |
Phone | +1(800)523-0502 |
Customer_Support@BD.com | |
Phone | +1(800)523-0502 |
Customer_Support@BD.com | |
Phone | +1(800)523-0502 |
Customer_Support@BD.com | |
Phone | +1(800)523-0502 |
Customer_Support@BD.com | |
Phone | +1(800)523-0502 |
Customer_Support@BD.com | |
Phone | +1(800)523-0502 |
Customer_Support@BD.com | |
Phone | +1(800)523-0502 |
Customer_Support@BD.com | |
Phone | +1(800)523-0502 |
Customer_Support@BD.com | |
Phone | +1(800)523-0502 |
Customer_Support@BD.com | |
Phone | +1(800)523-0502 |
Customer_Support@BD.com | |
Phone | +1(800)523-0502 |
Customer_Support@BD.com | |
Phone | +1(800)523-0502 |
Customer_Support@BD.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10885403184482 [Primary] |
GS1 | 50885403184480 [Package] Contains: 10885403184482 Package: Case [10 Units] Discontinued: 2023-09-30 Not in Commercial Distribution |
HGD | APPLICATOR, VAGINAL |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2024-02-23 |
Device Publish Date | 2018-07-18 |
10885403051722 - V. Mueller | 2024-05-03 LUMBAR AORTOGRAPHY NDL THINWALL 17GA 7IN |
10885403049408 - V. Mueller | 2024-05-01 V. Mueller LEFORT URETHRAL SOUND 8FR, THREADED 1/56" FOR STD FILIFORM (NOT INCLUDED) OVERALL LENGTH 11" (28CM) |
10885403071263 - V. Mueller | 2024-05-01 V. Mueller CHERRY S-SHAPED BRAIN RETRACTOR 10 AND 13MM WIDE OVERALL LENGTH 6-3/4" (17.1CM) |
10885403105159 - V. Mueller | 2024-05-01 V. Mueller CRAIG TOOTHED CUTTER ONLY FOR CRAIG BIOPSY SET OVERALL LENGTH 7-3/8" (18.7CM) |
20885403473170 - N/A | 2024-02-27 Surgical Clipper |
50885403142176 - Wet Exidine | 2024-02-23 Wet Exidine-4 (CHG 4%) Preoperative Skin Prep Tray |
50885403142183 - NA | 2024-02-23 Wet PVP-I Small Procedure Preoperative Skin Prep Tray |
50885403142190 - NA | 2024-02-23 Dry Preoperative Skin Prep Tray With Powder-Free Gloves |