Identity
- Trade Name
- T-POD(TM) Combat Pelvic Stabilization Device EUDAMEDARROW FDA UDI
- Generic Name
- Pelvic fracture binder, single-use FDA UDI
- Device Name
- T-POD PELVIC STABILIZATION DEVICE EUDAMEDT-POD(TM) Combat Pelvic Stabilization Device FDA UDI
- Model / Reference
- T-PODC EUDAMEDIPN915612 FDA UDI
- Description
- T-POD(TM) Combat Pelvic Stabilization Device FDA UDI
Identifiers
- Catalog Number
- T-PODC FDA UDI
- Primary DI / UDI-DI
- 14026704712769 EUDAMEDFDA UDI
- Basic UDI-DI
- 08019020000000000000021JY EUDAMED
- FDA Product Code
- IPY FDA UDI
- EMDN Code
- M030599 IMMOBILISATION SYSTEMS AND DEVICES - OTHER EUDAMED
- GMDN Term
- Pelvic fracture binder, single-use FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 890.3490 FDA UDI
- Market of Registration
- Ireland EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Pelvic fracture binder, single-use
Arrow by Teleflex Incorporated — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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Also classified as Pelvic fracture binder, single-use.
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Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class I | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Teleflex Incorporated
Sources (2)
- FDA UDI 4f45cec2-d968-4d5f-9625-733e804ba1d3 35 fields · synced Aug 3, 2026
- EUDAMED 5db9717f-051b-4ed4-945f-b4f04026fd82 61 fields · synced Aug 3, 2026