Primary Device ID | 01618125187170 |
NIH Device Record Key | 5b050430-be73-4951-b2d7-f1b2faf969e6 |
Commercial Distribution Discontinuation | 2022-09-22 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | GE Healthcare |
Version Model Number | 33306 |
Company DUNS | 063519193 |
Company Name | TIDI PRODUCTS, LLC |
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 | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 01618125187170 [Primary] |
KKX | Drape, Surgical |
Steralize Prior To Use | true |
Device Is Sterile | true |
[01618125187170]
Ethylene Oxide
[01618125187170]
Ethylene Oxide
[01618125187170]
Ethylene Oxide
[01618125187170]
Ethylene Oxide
[01618125187170]
Ethylene Oxide
[01618125187170]
Ethylene Oxide
[01618125187170]
Ethylene Oxide
[01618125187170]
Ethylene Oxide
[01618125187170]
Ethylene Oxide
[01618125187170]
Ethylene Oxide
[01618125187170]
Ethylene Oxide
[01618125187170]
Ethylene Oxide
[01618125187170]
Ethylene Oxide
[01618125187170]
Ethylene Oxide
[01618125187170]
Ethylene Oxide
[01618125187170]
Ethylene Oxide
[01618125187170]
Ethylene Oxide
[01618125187170]
Ethylene Oxide
[01618125187170]
Ethylene Oxide
[01618125187170]
Ethylene Oxide
[01618125187170]
Ethylene Oxide
[01618125187170]
Ethylene Oxide
[01618125187170]
Ethylene Oxide
[01618125187170]
Ethylene Oxide
[01618125187170]
Ethylene Oxide
[01618125187170]
Ethylene Oxide
[01618125187170]
Ethylene Oxide
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2024-07-25 |
Device Publish Date | 2017-09-18 |
00618125183579 | Elegance Mattress Pad, 1 Each |
00618125183562 | MRI Positioning Kit |
00618125178490 | REST, LEG, 10" X 24" X 18" |
00618125175925 | Pad, Table, OEC UroView 2800, 1 per Each |
00618125170739 | Ge Healthcare Patient Positioners 15.5in x 15.3in x 2in 2 per Set |
00618125162505 | CUSHION, LARGE INFANT HEAD, 1 per Each |
00618125162499 | CUSHION, MEDIUM INFANT HEAD, 1 per Each |
00618125162482 | CUSHION, SMALL INFANT HEAD, 1 per Each |
00618125146154 | Positioning Aids - Wedges 7.3in x 1in x 3in 1 per Each |
00618125146147 | WEDGE, AXIAL HEADHOLDER, 10° |
00618125145775 | Axial Head Holder, Foam |
00618125187195 | OEC ® Disposables, 9 inch Image Intensifier 9800, 9900 & Elite™ 21cm CFM, 10 per Case |
00618125187171 | 12"II 9900,9800 ELITE,31CM |
00618125187164 | OEC ® Disposables, 9 inch Image Intensifier 9800, 9900 & Elite™ 21cm CFM, 20 per Case |
00618125155279 | Sterile Mobile XR Tube Drape, 20 per Case |
10618125187185 | OEC Disposables, 12 inch Image Intensifer 9800, 9900, and Elite 31cm, 10 per Case |
10618125183859 | 4K Monitor Drape, Clear Polyethylene Sterile 20 per Case |
00618125187157 | Purple C-Bow Drape for 9900, 9800 Elite and CFM Elite, 20 per Case |
01618125187194 | OEC ® Disposables, 9 inch Image Intensifier 9800, 9900 & Elite™ 21cm CFM, 10 per Case |
01618125187187 | OEC Disposables, 12 inch Image Intensifer 9800, 9900, and Elite 31cm, 10 per Case |
01618125187170 | 12"II 9900,9800 ELITE,31CM |
01618125187163 | OEC ® Disposables, 9 inch Image Intensifier 9800, 9900 & Elite™ 21cm CFM, 20 per Case |
01618125183851 | 4K Monitor Drape, Clear Polyethylene Sterile 20 per Case |
01618125155278 | Sterile Mobile XR Tube Drape, 20 per Case |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
GE HEALTHCARE 97537319 not registered Live/Pending |
General Electric Company 2022-08-05 |
GE HEALTHCARE 97536608 not registered Live/Pending |
General Electric Company 2022-08-05 |