Identity
- Trade Name
- Arthrex® FDA UDI
- Generic Name
- Surgical support tape, bioabsorbable FDA UDI
- Device Name
- Scissor Punch, 2.5 x 260mm FDA UDI
- Model / Reference
- AR-S7116-025-260 FDA UDI
- Description
- Scissor Punch, 2.5 x 260mm FDA UDI
Identifiers
- Catalog Number
- AR-S7116-025-260 FDA UDI
- Primary DI / UDI-DI
- 00888867427488 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Surgical support tape, bioabsorbable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
Yes
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Surgical support tape, bioabsorbable
Arthrex® by Arthrex, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Surgical support tape, bioabsorbable.
- SUTUMED — Unilene Sac · Class II
- SUTUMED — Unilene Sac · Class II
- Arthrex® — Arthrex, Inc. · Class I
- Arthrex® — Arthrex, Inc. · 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
- Arthrex, Inc.
Sources (1)
- FDA UDI 302a1e23-c03c-4e59-a601-8a9e842de9b4 35 fields · synced May 29, 2026