Primary Device ID | 00887761001008 |
NIH Device Record Key | d80d88e3-3530-42a6-9d96-8a2adbf2a63f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | OB/GYN Stretcher |
Version Model Number | P8050H |
Company DUNS | 813030004 |
Company Name | Hill-Rom de México, S. de R.L. de C.V. |
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 | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00887761001008 [Primary] |
FPO | STRETCHER, WHEELED |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-17 |
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