Identity
- Trade Name
- Appose ULC FDA UDI
- Generic Name
- Skin stapler/staple, non-bioabsorbable FDA UDI
- Device Name
- Slim Body Skin Stapler FDA UDI
- Model / Reference
- 8886803712 FDA UDI
- Description
- Slim Body Skin Stapler FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10884521104372 FDA UDI
- FDA Product Code
- GDT FDA UDI
- GMDN Term
- Skin stapler/staple, non-bioabsorbable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4760 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Conditional FDA UDI
Category: Skin stapler/staple, non-bioabsorbable
Appose ULC by Covidien LP — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Skin stapler/staple, non-bioabsorbable.
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- WECK — TELEFLEX INCORPORATED · Class I
- citec — Changzhou Intl. Trade & Enterprises Cooperative Co., Ltd. · Class I
- CD HORIZON® Spinal System — MEDTRONIC SOFAMOR DANEK, INC. · Class II
- SkinPlus — Taiwan Surgical Corporation · Class I
- TSRH® Spinal System — MEDTRONIC SOFAMOR DANEK, INC. · Class II
- REFLEX — Conmed Corporation · Class I
- WECK — TELEFLEX INCORPORATED · 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
- Covidien LP
Sources (1)
- FDA UDI 37cf5e76-6b4f-4e71-9666-183187aedea3 36 fields · synced Jun 8, 2026