Identity
- Trade Name
- Medline FDA UDI
- Generic Name
- Manual scalpel blade, single-use FDA UDI
- Device Name
- BLADE,STAINLESS-STEEL,22,STRL,DISPOSABLE FDA UDI
- Model / Reference
- CISION22SS FDA UDI
- Description
- BLADE,STAINLESS-STEEL,22,STRL,DISPOSABLE FDA UDI
Identifiers
- Catalog Number
- CISION22SS FDA UDI
- Primary DI / UDI-DI
- 30193489090288 FDA UDI
- FDA Product Code
- GES FDA UDI
- GMDN Term
- Manual scalpel blade, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
Category: Manual scalpel blade, single-use
Medline by Medline Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Manual scalpel blade, single-use.
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- Sterile Stainless Blades — Southmedic Incorporated · Class I
- Paramount — Paramount Surgimed Limited · Class IIa
- Swann-Morton — Swann-Morton Ltd · Class IIa
- SHARD — APPLIED DENTAL, 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
- Medline Industries, Inc.
Sources (1)
- FDA UDI dea20d23-64ae-4222-ac06-89dbd2942f57 35 fields · synced Jun 6, 2026