Primary Device ID | 04046964152306 |
NIH Device Record Key | e9a3de77-b6e5-4bbf-a8de-e5890ab704e2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Plasmafit® Pro 3 |
Version Model Number | NV852T |
Catalog Number | NV852T |
Company DUNS | 315018218 |
Company Name | Aesculap AG |
Device Count | 1 |
DM Exempt | false |
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 | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(888)229-3002 |
setworld_orders@aesculap.com | |
Phone | +1(888)229-3002 |
setworld_orders@aesculap.com | |
Phone | +1(888)229-3002 |
setworld_orders@aesculap.com | |
Phone | +1(888)229-3002 |
setworld_orders@aesculap.com | |
Phone | +1(888)229-3002 |
setworld_orders@aesculap.com | |
Phone | +1(888)229-3002 |
setworld_orders@aesculap.com | |
Phone | +1(888)229-3002 |
setworld_orders@aesculap.com | |
Phone | +1(888)229-3002 |
setworld_orders@aesculap.com | |
Phone | +1(888)229-3002 |
setworld_orders@aesculap.com | |
Phone | +1(888)229-3002 |
setworld_orders@aesculap.com | |
Phone | +1(888)229-3002 |
setworld_orders@aesculap.com | |
Phone | +1(888)229-3002 |
setworld_orders@aesculap.com | |
Phone | +1(888)229-3002 |
setworld_orders@aesculap.com |
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 | 04046964152306 [Primary] |
OQG | Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-09-09 |
Device Publish Date | 2015-11-11 |
04046964152399 | PLASMAFIT PRO 3 CUP SIZE 70MM K |
04046964152382 | PLASMAFIT PRO 3 CUP SIZE 68MM K |
04046964152375 | PLASMAFIT PRO 3 CUP SIZE 66MM K |
04046964152368 | PLASMAFIT PRO 3 CUP SIZE 64MM K |
04046964152351 | PLASMAFIT PRO 3 CUP SIZE 62MM J |
04046964152344 | PLASMAFIT PRO 3 CUP SIZE 60MM J |
04046964152337 | PLASMAFIT PRO 3 CUP SIZE 58MM J |
04046964152320 | PLASMAFIT PRO 3 CUP SIZE 56MM I |
04046964152313 | PLASMAFIT PRO 3 CUP SIZE 54MM H |
04046964152306 | PLASMAFIT PRO 3 CUP SIZE 52MM G |
04046964152290 | PLASMAFIT PRO 3 CUP SIZE 50MM F |
04046964152283 | PLASMAFIT PRO 3 CUP SIZE 48MM E |
04046964152276 | PLASMAFIT PRO 3 CUP SIZE 46MM D |
04046964152269 | PLASMAFIT PRO 3 CUP SIZE 44MM C |
04046964152252 | PLASMAFIT PRO 3 CUP SIZE 42MM B |
04046964152245 | PLASMAFIT PRO 3 CUP SIZE 40MM A |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PLASMAFIT 97248230 not registered Live/Pending |
Aesculap AG 2022-02-01 |
PLASMAFIT 85665326 not registered Dead/Abandoned |
Aesculap AG 2012-06-29 |