Identity
- Trade Name
- Arch Assembly FDA UDI
- Generic Name
- Stretcher equipment holder FDA UDI
- Device Name
- ASSEMBLY, ACCESSORY ARCH, TS SLED, KA FDA UDI
- Model / Reference
- AR2-043-01 FDA UDI
- Description
- ASSEMBLY, ACCESSORY ARCH, TS SLED, KA FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00810050863124 FDA UDI
- FDA Product Code
- FOX FDA UDI
- GMDN Term
- Stretcher equipment holder FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6990 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Stretcher equipment holder
Arch Assembly by Lifeport, Llc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Stretcher equipment holder.
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- Arch Assembly — LIFEPORT, LLC. · Class I
- Arch Assembly — LIFEPORT, LLC. · Class I
- Arch Assembly — LIFEPORT, LLC. · Class I
- Arch Assembly — LIFEPORT, LLC. · Class I
- Arch Assembly — LIFEPORT, LLC. · Class I
- Arch Assembly — LIFEPORT, LLC. · Class I
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 I | Pending data |
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Manufacturer
- Manufacturer
- Lifeport, Llc.
Sources (1)
- FDA UDI ea3464f2-a30f-44ca-9828-3a2aeffbe72c 34 fields · synced May 30, 2026