Primary Device ID | 05060097930692 |
NIH Device Record Key | 8f5a0b70-6c0b-4ed3-9fef-094ae081a2d6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Biogel Eclipse® |
Version Model Number | 75280 |
Company DUNS | 631770658 |
Company Name | Mölnlycke Health Care AB |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | false |
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 | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | true |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05060097930531 [Primary] |
GS1 | 05060097930616 [Package] Contains: 05060097930531 Package: PACK_OR_INNER_PACK [50 Units] In Commercial Distribution |
GS1 | 05060097930692 [Package] Contains: 05060097930616 Package: CASE [4 Units] In Commercial Distribution |
KGO | Surgeon's gloves |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-10-31 |
Device Publish Date | 2022-10-21 |
05060097930715 | Biogel Eclipse 9.0 x40 US |
05060097930708 | Biogel Eclipse 8.5 x50 US |
05060097930692 | Biogel Eclipse 8.0 x50 US |
05060097930685 | Biogel Eclipse 7.5 x50 US |
05060097930678 | Biogel Eclipse 7.0 x50 US |
05060097930661 | Biogel Eclipse 6.5 x50 US |
05060097930654 | Biogel Eclipse 6.0 x50 US |
05060097930562 | Biogel Eclipse 5.5 x50 US |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BIOGEL ECLIPSE 78534254 3357132 Live/Registered |
Regent Medical Limited 2004-12-17 |