Identity
- Trade Name
- t:flex Insulin Pump, Replacement, Refurbished FDA UDI
- Generic Name
- Ambulatory insulin infusion pump reservoir FDA UDI
- Device Name
- Assembly, Pump Replacement, Refurbished, t:flex FDA UDI
- Model / Reference
- 007473 FDA UDI
- Description
- Assembly, Pump Replacement, Refurbished, t:flex FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00852162004569 FDA UDI
- FDA Product Code
- LZG FDA UDI
- GMDN Term
- Ambulatory insulin infusion pump reservoir FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5725 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Unsafe FDA UDI
Dimensions & Sizes
- Size
- Total Volume — 4.8 Milliliter FDA UDI
Category: Ambulatory insulin infusion pump reservoir
t:flex Insulin Pump, Replacement, Refurbished by Tandem Diabetes Care, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Ambulatory insulin infusion pump reservoir.
- iLet Insulin Infusion Kit - Inset (23”, 6mm) 15-Pack (Pharmacy Kit) — Beta Bionics, Inc. · Class II
- MiniMed Reservoir — MEDTRONIC MINIMED, INC. · Class II
- MiniMed™ Reservoir — MEDTRONIC MINIMED, INC. · Class III
- DANA Diabecare — SOOIL DEVELOPMENT CO., LTD · Class II
- iLet Insulin Infusion Kit - Inset (32”, 6mm) 15-Pack (Pharmacy Kit) — Beta Bionics, Inc. · Class II
- iLet Starter Kit - Contact Detach — Beta Bionics, Inc. · Class II
- CeQur Simplicity — Cequr SA · Class II
- iLet Insulin Infusion Kit – Contact Detach™ (23"", 6mm) - 20-Pack — Beta Bionics, Inc. · Class II
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Tandem Diabetes Care, Inc.
Sources (1)
- FDA UDI 88bcdb27-5ce9-41e3-a262-c7255d8cbd24 36 fields · synced Jun 8, 2026