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Tcc-Ez®
FDA UDIEUDAMEDClass I (US FDA UDI)
Ref TP-1102Model Sterile Wound Closure Strips
by Acell, Inc.
Identity
- Trade Name
- Suture Strip Plus EUDAMEDTCC-EZ® FDA UDI
- Generic Name
- Cast cutter blade FDA UDI
- Device Name
- TOTAL CONTACT CAST SYSTEM - Cast Removal Saw Replacement Stell Blades. FDA UDI
- Model / Reference
- Sterile Wound Closure Strips EUDAMEDTP-1102 EUDAMEDTCC2SAWSSB FDA UDI
- Description
- TOTAL CONTACT CAST SYSTEM - Cast Removal Saw Replacement Stell Blades. FDA UDI
Identifiers
- Catalog Number
- TCC2SAWSSB FDA UDI
- Primary DI / UDI-DI
- 00809958000373 EUDAMEDFDA UDI
- Basic UDI-DI
- 0809958MDRTD0058Q EUDAMED
- Direct Marketing DI
- 00809958000373 EUDAMED
- FDA Product Code
- LGH FDA UDI
- EMDN Code
- H90020199 SUTURE TAPES - OTHER EUDAMED
- GMDN Term
- Cast cutter blade FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 888.5960 FDA UDI
- Market of Registration
- Netherlands EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
EUDAMEDFDA UDI
Single Use
No
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
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Cast cutter blade
Tcc-Ez® by Acell, Inc. — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Acell, Inc.
Sources (2)
- FDA UDI 01cc4be3-b5cc-4868-83f0-87fc19059001 35 fields · synced Jul 9, 2026
- EUDAMED 727b5f7b-03b3-40d3-99e8-28c8fe12bee9 61 fields · synced Jul 9, 2026