INDUSTRIAS GRAYLING DE MEXICO, SA DE C

FDA Device Registration & Listing · Juarez Chihuahua, MX · Registration 3032012299

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3032012299
FEI Number
3032012299
Entity Name
INDUSTRIAS GRAYLING DE MEXICO, SA DE C
City/State/Country
Juarez Chihuahua, MX
Establishment Address
Eje Juan Gabriel 2255, Juarez Chihuahua 32380, MX
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Industrias Grayling de Mexico, SA de C (Owner Number: 10091649)
Owner / Operator Contact Address
Eje Juan Gabriel 2255, Juarez, MX-CHH 32380, MX
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Silhouette Circuits – C-1781-MD – SIL II MEDIUM CIRCUIT / Silhouette 2 Circuit, Medium Silhouette Circuits – C-1781-PD – SIL II PEDIATRIC CIRCUIT / Silhouette 2 Circuit, Pediatric Silhouette Circuits – C-1781-LG – SIL II LARGE CIRCUIT / Silhouette Circuit, Large Silhouette Circuits – C-1781-SM – SIL II SMALL CIRCUIT / Silhouette 2 Circuit, Small

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CAI Circuit, Breathing (W Connector, Adaptor, Y Piece) Anesthesiology Class 1 868.5240 2024-10-21

Official Correspondent

Sommer Altvater

US Agent Details

Sommer Altvater Email: sommer.altvater@irco.com Phone: (302) 3045416

Related Public Records

Same Entity

Industrias Grayling de Mexico, SA de C
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0033-04 VIASYS Med Systems 1
Neonatal/Infant Hyperinflation Circuit, consisting of a 0.5 L breathing bag, pressure monitoring tube with Bird adapter, oxygen supply tubing, sideport connector with adjustable bleed valve, and 40 cm H2O Popoff elbow; Mfg. for Corpak MedSystems, Wheeling, IL 60090; 20 units per case; reorder #BLD-83124-2
Z-0034-04 VIASYS Med Systems 1
Neonatal/Infant Hyperinflation Circuit, consisting of a 0.5 L breathing bag, pressure monitoring tube, oxygen supply tubing, sideport connector with adjustable bleed valve, ported elbow and infant mask; Mfg. for Corpak MedSystems, Wheeling, IL 60090; 20 units per case; reorder #BLD-83100-24
Z-0035-04 VIASYS Med Systems 1
Neonatal/Infant Hyperinflation Circuit, consisting of a 0.5 L breathing bag, pressure monitoring tube, oxygen supply tubing, sideport connector with adjustable bleed valve, 40 cm H2O Popoff elbow and infant mask; Mfg. for Corpak MedSystems, Wheeling, IL 60090; 20 units per case; reorder #BLD-83144-24
Z-0036-04 VIASYS Med Systems 1
Hyperinflation Circuit, consisting of a 2.0 L breathing bag, pressure monitoring tube, oxygen supply tubing, sideport connector with adjustable bleed valve and ported elbow; Mfg. for Corpak MedSystems, Wheeling, IL 60090; 20 units per case; reorder #BLD-83120
Z-0037-04 VIASYS Med Systems 1
Sideport Kit, consisting of an adjustable sideport valve and an O2 port elbow; Mfg. for Corpak MedSystems, Wheeling, IL 60090; 20 units per case; reorder #BLD-83166

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3032012299. Last updated year: 2026. Please use registration number 3032012299 when referencing this establishment in official correspondence.
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