Identity
- Trade Name
- PERMA PURE FDA UDI
- Generic Name
- Gas-sampling/monitoring respiratory tubing, single-use FDA UDI
- Device Name
- ME-070-03-24 36" ME with Male Luers FDA UDI
- Model / Reference
- ME Series FDA UDI
- Description
- ME-070-03-24 36" ME with Male Luers FDA UDI
Identifiers
- Catalog Number
- ME-070-03-24 FDA UDI
- Primary DI / UDI-DI
- 00840106906086 FDA UDI
- FDA Product Code
- CBQ FDA UDI
- GMDN Term
- Gas-sampling/monitoring respiratory tubing, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.1500 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Gas-sampling/monitoring respiratory tubing, single-use
Perma Pure by Perma Pure, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Perma Pure, LLC
Sources (1)
- FDA UDI bcff1edc-07f8-4dd4-a189-7fb490cb8cfd 34 fields · synced Jun 8, 2026