Identity
- Trade Name
- In-Situ Deluxe Superfine Double Layer Large FDA UDI
- Generic Name
- General-purpose patient lifting system sling/harness FDA UDI
- Model / Reference
- M921536-L FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05056387439549 FDA UDI
- FDA Product Code
- INE FDA UDI
- GMDN Term
- General-purpose patient lifting system sling/harness FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.3910 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: General-purpose patient lifting system sling/harness
In-Situ Deluxe Superfine Double Layer Large by Silvalea Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as General-purpose patient lifting system sling/harness.
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- Apex Lifts — Joerns Healthcare · Class I
- Long Seat - Tollos — 1073849 Ontario Limited · Class I
- Slings — Joerns Healthcare · Class I
- Accessories — Joerns Healthcare · Class I
- EZ Way — EZ Way, Inc. · Class I
- Sage TAP LC — SAGE PRODUCTS LLC · 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
- Silvalea Limited
Sources (1)
- FDA UDI 72e5c259-f439-4a06-b811-a6d233c9d9b0 32 fields · synced May 31, 2026